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How to Do Well in Organic Chemistry: One Student’s Advice
Last updated: January 23rd, 2024 |
Over at Med School Odyssey, the author recently wrote about finishing Org 1, and has a lot to share about his experiences with the course. Here are some choice excerpts from that post, and from a few of his earlier posts.
1. Don’t believe the hype
Don’t let yourself get psyched out by the people around you whining about how difficult organic chemistry is. I let myself get taken in by the horror stories around the first exam and did substantially worse on the first exam than I should have simply because I bought into the idea that it was tough and I was going to fail. I learned a lot more about myself and self-confidence during the first few weeks than I did about chemistry. If you’re surrounded by negative and pessimistic people, tell them to piss off – don’t get sucked into their game. Prepare and study well – play your game, not theirs.
2. Focus on understanding, not memorization
I have no idea where people get the idea that organic chemistry is memorization. I didn’t make a single notecard for the entire course – I don’t even know what you would even memorize. Anyone that tells you organic chemistry requires gobs of memorization is seriously misinformed.
I agree with the sentiment here. I’d say that memorization is, overall, a poor strategy that is resorted to when people haven’t planned ahead sufficiently and have to cram the night before an exam. There are, however, certain aspects of the course that require memorization – like nomenclature terms, reagent names and acronmys, functional groups, and so on. While some people indeed might have these terms wired in after a few weeks of the course, others might have to resort to flash cards or other memory-centered devices in order to retain the course material. There’s nothing wrong with that, as long as it’s coupled with a dedication toward understanding the deeper concepts.
3. A Physics Background Really Helps.
I’m convinced that a year of physics, even if only at a conceptual level (ie., without all the math), would make organic chemistry a lot easier. Understanding transition states, activation energies, conformational changes, and a host of other things in organic chemistry would be a lot easier with an understanding of some basic physics. My advice to organic chemistry students that want to really stack the deck in their favor: wait until you’ve had the entire physics sequence before taking organic chemistry.
If you’ve glanced at the “From Gen Chem to Organic Chem” series I put together this summer, one thing you’ll notice is just how much physics lies behind a lot of organic chemistry phenomena. In particular, a good understanding of electrostatics will make a huge difference. In addition, familiarity with the basics of thermodynamics, equilibria, and kinetics will be invaluable when trying to grasp the topics you encounter in Org 1.
4. Good Study Habits Are Key
Two good quotes here. Quote #1:
This was the primary reason I saw people fail organic chemistry. It wasn’t intelligence. It wasn’t lack of memorization abilities. It wasn’t the teaching. It was their study habits.There was a group of about seven girls in the back of our class, the ‘Chatty Kathys’, that waited until the night before the homework was due to start on it and didn’t do any outside reading or problems on their own. I doubt they failed, but they probably comprised the bulk of the C grades in the course. Organic isn’t hard, but that doesn’t mean you can just sit in lecture and expect to have the understanding and ability to solve problems to just leap inside your head. Maybe that’s part of why medical schools scrutinize organic chemistry grades so much – it definitely reveals the quality of your study habits.
Quote #2:
I don’t know anyone for whom learning organic chemistry is easy. The top five students in my class probably spent 20 hours every week studying for the class. I would say that organic chemistry came somewhat easier for me, but it still required me to put in a huge amount of time.
No surprises here. Note that the good students still have to bust their butts to do well. There are no Val Kilmer in “Real Genius”-like stories of students walking into an exam unprepared and acing it. It doesn’t happen. It takes a lot of fricking work to do well.
5. The Bottom Line
The keys to success: be prepared, focus on understanding, work enough problems outside of class to learn the concepts – you’ll never learn the concepts unless you make mistakes on problems and learn from them – and stay caught up with the material.
Does this sound familiar? It sounds a lot like a lot of the collected advice professors give to their students on the first day of class – not to mention the advice students who just finished Org 1 would give themselves if they could go back in time to the beginning of the course.
In short, there’s no magic to doing well in the course. It involves discipline, putting in time consistently, doing problems, focusing on learning concepts, and staying on top of the material. If it sounds disappointing that there’s no magic formula for success, it should at least be comforting that doing well in the course is very possible for averagely gifted students who put in the time and study effectively.
00 General Chemistry Review
01 Bonding, Structure, and Resonance
- How Do We Know Methane (CH4) Is Tetrahedral?
- Hybrid Orbitals and Hybridization
- How To Determine Hybridization: A Shortcut
- Orbital Hybridization And Bond Strengths
- Sigma bonds come in six varieties: Pi bonds come in one
- A Key Skill: How to Calculate Formal Charge
- The Four Intermolecular Forces and How They Affect Boiling Points
- 3 Trends That Affect Boiling Points
- How To Use Electronegativity To Determine Electron Density (and why NOT to trust formal charge)
- Introduction to Resonance
- How To Use Curved Arrows To Interchange Resonance Forms
- Evaluating Resonance Forms (1) - The Rule of Least Charges
- How To Find The Best Resonance Structure By Applying Electronegativity
- Evaluating Resonance Structures With Negative Charges
- Evaluating Resonance Structures With Positive Charge
- Exploring Resonance: Pi-Donation
- Exploring Resonance: Pi-acceptors
- In Summary: Evaluating Resonance Structures
- Drawing Resonance Structures: 3 Common Mistakes To Avoid
- How to apply electronegativity and resonance to understand reactivity
- Bond Hybridization Practice
- Structure and Bonding Practice Quizzes
- Resonance Structures Practice
02 Acid Base Reactions
- Introduction to Acid-Base Reactions
- Acid Base Reactions In Organic Chemistry
- The Stronger The Acid, The Weaker The Conjugate Base
- Walkthrough of Acid-Base Reactions (3) - Acidity Trends
- Five Key Factors That Influence Acidity
- Acid-Base Reactions: Introducing Ka and pKa
- How to Use a pKa Table
- The pKa Table Is Your Friend
- A Handy Rule of Thumb for Acid-Base Reactions
- Acid Base Reactions Are Fast
- pKa Values Span 60 Orders Of Magnitude
- How Protonation and Deprotonation Affect Reactivity
- Acid Base Practice Problems
03 Alkanes and Nomenclature
- Meet the (Most Important) Functional Groups
- Condensed Formulas: Deciphering What the Brackets Mean
- Hidden Hydrogens, Hidden Lone Pairs, Hidden Counterions
- Don't Be Futyl, Learn The Butyls
- Primary, Secondary, Tertiary, Quaternary In Organic Chemistry
- Branching, and Its Affect On Melting and Boiling Points
- The Many, Many Ways of Drawing Butane
- Wedge And Dash Convention For Tetrahedral Carbon
- Common Mistakes in Organic Chemistry: Pentavalent Carbon
- Table of Functional Group Priorities for Nomenclature
- Summary Sheet - Alkane Nomenclature
- Organic Chemistry IUPAC Nomenclature Demystified With A Simple Puzzle Piece Approach
- Boiling Point Quizzes
- Organic Chemistry Nomenclature Quizzes
04 Conformations and Cycloalkanes
- Staggered vs Eclipsed Conformations of Ethane
- Conformational Isomers of Propane
- Newman Projection of Butane (and Gauche Conformation)
- Introduction to Cycloalkanes (1)
- Geometric Isomers In Small Rings: Cis And Trans Cycloalkanes
- Calculation of Ring Strain In Cycloalkanes
- Cycloalkanes - Ring Strain In Cyclopropane And Cyclobutane
- Cyclohexane Conformations
- Cyclohexane Chair Conformation: An Aerial Tour
- How To Draw The Cyclohexane Chair Conformation
- The Cyclohexane Chair Flip
- The Cyclohexane Chair Flip - Energy Diagram
- Substituted Cyclohexanes - Axial vs Equatorial
- Ranking The Bulkiness Of Substituents On Cyclohexanes: "A-Values"
- Cyclohexane Chair Conformation Stability: Which One Is Lower Energy?
- Fused Rings - Cis-Decalin and Trans-Decalin
- Naming Bicyclic Compounds - Fused, Bridged, and Spiro
- Bredt's Rule (And Summary of Cycloalkanes)
- Newman Projection Practice
- Cycloalkanes Practice Problems
05 A Primer On Organic Reactions
- The Most Important Question To Ask When Learning a New Reaction
- Learning New Reactions: How Do The Electrons Move?
- The Third Most Important Question to Ask When Learning A New Reaction
- 7 Factors that stabilize negative charge in organic chemistry
- 7 Factors That Stabilize Positive Charge in Organic Chemistry
- Nucleophiles and Electrophiles
- Curved Arrows (for reactions)
- Curved Arrows (2): Initial Tails and Final Heads
- Nucleophilicity vs. Basicity
- The Three Classes of Nucleophiles
- What Makes A Good Nucleophile?
- What makes a good leaving group?
- 3 Factors That Stabilize Carbocations
- Equilibrium and Energy Relationships
- What's a Transition State?
- Hammond's Postulate
- Learning Organic Chemistry Reactions: A Checklist (PDF)
- Introduction to Free Radical Substitution Reactions
- Introduction to Oxidative Cleavage Reactions
06 Free Radical Reactions
- Bond Dissociation Energies = Homolytic Cleavage
- Free Radical Reactions
- 3 Factors That Stabilize Free Radicals
- What Factors Destabilize Free Radicals?
- Bond Strengths And Radical Stability
- Free Radical Initiation: Why Is "Light" Or "Heat" Required?
- Initiation, Propagation, Termination
- Monochlorination Products Of Propane, Pentane, And Other Alkanes
- Selectivity In Free Radical Reactions
- Selectivity in Free Radical Reactions: Bromination vs. Chlorination
- Halogenation At Tiffany's
- Allylic Bromination
- Bonus Topic: Allylic Rearrangements
- In Summary: Free Radicals
- Synthesis (2) - Reactions of Alkanes
- Free Radicals Practice Quizzes
07 Stereochemistry and Chirality
- Types of Isomers: Constitutional Isomers, Stereoisomers, Enantiomers, and Diastereomers
- How To Draw The Enantiomer Of A Chiral Molecule
- How To Draw A Bond Rotation
- Introduction to Assigning (R) and (S): The Cahn-Ingold-Prelog Rules
- Assigning Cahn-Ingold-Prelog (CIP) Priorities (2) - The Method of Dots
- Enantiomers vs Diastereomers vs The Same? Two Methods For Solving Problems
- Assigning R/S To Newman Projections (And Converting Newman To Line Diagrams)
- How To Determine R and S Configurations On A Fischer Projection
- The Meso Trap
- Optical Rotation, Optical Activity, and Specific Rotation
- Optical Purity and Enantiomeric Excess
- What's a Racemic Mixture?
- Chiral Allenes And Chiral Axes
- Stereochemistry Practice Problems and Quizzes
08 Substitution Reactions
- Introduction to Nucleophilic Substitution Reactions
- Walkthrough of Substitution Reactions (1) - Introduction
- Two Types of Nucleophilic Substitution Reactions
- The SN2 Mechanism
- Why the SN2 Reaction Is Powerful
- The SN1 Mechanism
- The Conjugate Acid Is A Better Leaving Group
- Comparing the SN1 and SN2 Reactions
- Polar Protic? Polar Aprotic? Nonpolar? All About Solvents
- Steric Hindrance is Like a Fat Goalie
- Common Blind Spot: Intramolecular Reactions
- The Conjugate Base is Always a Stronger Nucleophile
- Substitution Practice - SN1
- Substitution Practice - SN2
09 Elimination Reactions
- Elimination Reactions (1): Introduction And The Key Pattern
- Elimination Reactions (2): The Zaitsev Rule
- Elimination Reactions Are Favored By Heat
- Two Elimination Reaction Patterns
- The E1 Reaction
- The E2 Mechanism
- E1 vs E2: Comparing the E1 and E2 Reactions
- Antiperiplanar Relationships: The E2 Reaction and Cyclohexane Rings
- Bulky Bases in Elimination Reactions
- Comparing the E1 vs SN1 Reactions
- Elimination (E1) Reactions With Rearrangements
- E1cB - Elimination (Unimolecular) Conjugate Base
- Elimination (E1) Practice Problems And Solutions
- Elimination (E2) Practice Problems and Solutions
10 Rearrangements
11 SN1/SN2/E1/E2 Decision
- Identifying Where Substitution and Elimination Reactions Happen
- Deciding SN1/SN2/E1/E2 (1) - The Substrate
- Deciding SN1/SN2/E1/E2 (2) - The Nucleophile/Base
- SN1 vs E1 and SN2 vs E2 : The Temperature
- Deciding SN1/SN2/E1/E2 - The Solvent
- Wrapup: The Key Factors For Determining SN1/SN2/E1/E2
- Alkyl Halide Reaction Map And Summary
- SN1 SN2 E1 E2 Practice Problems
12 Alkene Reactions
- E and Z Notation For Alkenes (+ Cis/Trans)
- Alkene Stability
- Alkene Addition Reactions: "Regioselectivity" and "Stereoselectivity" (Syn/Anti)
- Stereoselective and Stereospecific Reactions
- Hydrohalogenation of Alkenes and Markovnikov's Rule
- Hydration of Alkenes With Aqueous Acid
- Rearrangements in Alkene Addition Reactions
- Halogenation of Alkenes and Halohydrin Formation
- Oxymercuration Demercuration of Alkenes
- Hydroboration Oxidation of Alkenes
- m-CPBA (meta-chloroperoxybenzoic acid)
- OsO4 (Osmium Tetroxide) for Dihydroxylation of Alkenes
- Palladium on Carbon (Pd/C) for Catalytic Hydrogenation of Alkenes
- Cyclopropanation of Alkenes
- A Fourth Alkene Addition Pattern - Free Radical Addition
- Alkene Reactions: Ozonolysis
- Summary: Three Key Families Of Alkene Reaction Mechanisms
- Synthesis (4) - Alkene Reaction Map, Including Alkyl Halide Reactions
- Alkene Reactions Practice Problems
13 Alkyne Reactions
- Acetylides from Alkynes, And Substitution Reactions of Acetylides
- Partial Reduction of Alkynes With Lindlar's Catalyst
- Partial Reduction of Alkynes With Na/NH3 To Obtain Trans Alkenes
- Alkyne Hydroboration With "R2BH"
- Hydration and Oxymercuration of Alkynes
- Hydrohalogenation of Alkynes
- Alkyne Halogenation: Bromination, Chlorination, and Iodination of Alkynes
- Alkyne Reactions - The "Concerted" Pathway
- Alkenes To Alkynes Via Halogenation And Elimination Reactions
- Alkynes Are A Blank Canvas
- Synthesis (5) - Reactions of Alkynes
- Alkyne Reactions Practice Problems With Answers
14 Alcohols, Epoxides and Ethers
- Alcohols - Nomenclature and Properties
- Alcohols Can Act As Acids Or Bases (And Why It Matters)
- Alcohols - Acidity and Basicity
- The Williamson Ether Synthesis
- Ethers From Alkenes, Tertiary Alkyl Halides and Alkoxymercuration
- Alcohols To Ethers via Acid Catalysis
- Cleavage Of Ethers With Acid
- Epoxides - The Outlier Of The Ether Family
- Opening of Epoxides With Acid
- Epoxide Ring Opening With Base
- Making Alkyl Halides From Alcohols
- Tosylates And Mesylates
- PBr3 and SOCl2
- Elimination Reactions of Alcohols
- Elimination of Alcohols To Alkenes With POCl3
- Alcohol Oxidation: "Strong" and "Weak" Oxidants
- Demystifying The Mechanisms of Alcohol Oxidations
- Protecting Groups For Alcohols
- Thiols And Thioethers
- Calculating the oxidation state of a carbon
- Oxidation and Reduction in Organic Chemistry
- Oxidation Ladders
- SOCl2 Mechanism For Alcohols To Alkyl Halides: SN2 versus SNi
- Alcohol Reactions Roadmap (PDF)
- Alcohol Reaction Practice Problems
- Epoxide Reaction Quizzes
- Oxidation and Reduction Practice Quizzes
15 Organometallics
- What's An Organometallic?
- Formation of Grignard and Organolithium Reagents
- Organometallics Are Strong Bases
- Reactions of Grignard Reagents
- Protecting Groups In Grignard Reactions
- Synthesis Problems Involving Grignard Reagents
- Grignard Reactions And Synthesis (2)
- Organocuprates (Gilman Reagents): How They're Made
- Gilman Reagents (Organocuprates): What They're Used For
- The Heck, Suzuki, and Olefin Metathesis Reactions (And Why They Don't Belong In Most Introductory Organic Chemistry Courses)
- Reaction Map: Reactions of Organometallics
- Grignard Practice Problems
16 Spectroscopy
- Degrees of Unsaturation (or IHD, Index of Hydrogen Deficiency)
- Conjugation And Color (+ How Bleach Works)
- Introduction To UV-Vis Spectroscopy
- UV-Vis Spectroscopy: Absorbance of Carbonyls
- UV-Vis Spectroscopy: Practice Questions
- Bond Vibrations, Infrared Spectroscopy, and the "Ball and Spring" Model
- Infrared Spectroscopy: A Quick Primer On Interpreting Spectra
- IR Spectroscopy: 4 Practice Problems
- 1H NMR: How Many Signals?
- Homotopic, Enantiotopic, Diastereotopic
- Diastereotopic Protons in 1H NMR Spectroscopy: Examples
- C13 NMR - How Many Signals
- Liquid Gold: Pheromones In Doe Urine
- Natural Product Isolation (1) - Extraction
- Natural Product Isolation (2) - Purification Techniques, An Overview
- Structure Determination Case Study: Deer Tarsal Gland Pheromone
17 Dienes and MO Theory
- What To Expect In Organic Chemistry 2
- Are these molecules conjugated?
- Conjugation And Resonance In Organic Chemistry
- Bonding And Antibonding Pi Orbitals
- Molecular Orbitals of The Allyl Cation, Allyl Radical, and Allyl Anion
- Pi Molecular Orbitals of Butadiene
- Reactions of Dienes: 1,2 and 1,4 Addition
- Thermodynamic and Kinetic Products
- More On 1,2 and 1,4 Additions To Dienes
- s-cis and s-trans
- The Diels-Alder Reaction
- Cyclic Dienes and Dienophiles in the Diels-Alder Reaction
- Stereochemistry of the Diels-Alder Reaction
- Exo vs Endo Products In The Diels Alder: How To Tell Them Apart
- HOMO and LUMO In the Diels Alder Reaction
- Why Are Endo vs Exo Products Favored in the Diels-Alder Reaction?
- Diels-Alder Reaction: Kinetic and Thermodynamic Control
- The Retro Diels-Alder Reaction
- The Intramolecular Diels Alder Reaction
- Regiochemistry In The Diels-Alder Reaction
- The Cope and Claisen Rearrangements
- Electrocyclic Reactions
- Electrocyclic Ring Opening And Closure (2) - Six (or Eight) Pi Electrons
- Diels Alder Practice Problems
- Molecular Orbital Theory Practice
18 Aromaticity
- Introduction To Aromaticity
- Rules For Aromaticity
- Huckel's Rule: What Does 4n+2 Mean?
- Aromatic, Non-Aromatic, or Antiaromatic? Some Practice Problems
- Antiaromatic Compounds and Antiaromaticity
- The Pi Molecular Orbitals of Benzene
- The Pi Molecular Orbitals of Cyclobutadiene
- Frost Circles
- Aromaticity Practice Quizzes
19 Reactions of Aromatic Molecules
- Electrophilic Aromatic Substitution: Introduction
- Activating and Deactivating Groups In Electrophilic Aromatic Substitution
- Electrophilic Aromatic Substitution - The Mechanism
- Ortho-, Para- and Meta- Directors in Electrophilic Aromatic Substitution
- Understanding Ortho, Para, and Meta Directors
- Why are halogens ortho- para- directors?
- Disubstituted Benzenes: The Strongest Electron-Donor "Wins"
- Electrophilic Aromatic Substitutions (1) - Halogenation of Benzene
- Electrophilic Aromatic Substitutions (2) - Nitration and Sulfonation
- EAS Reactions (3) - Friedel-Crafts Acylation and Friedel-Crafts Alkylation
- Intramolecular Friedel-Crafts Reactions
- Nucleophilic Aromatic Substitution (NAS)
- Nucleophilic Aromatic Substitution (2) - The Benzyne Mechanism
- Reactions on the "Benzylic" Carbon: Bromination And Oxidation
- The Wolff-Kishner, Clemmensen, And Other Carbonyl Reductions
- More Reactions on the Aromatic Sidechain: Reduction of Nitro Groups and the Baeyer Villiger
- Aromatic Synthesis (1) - "Order Of Operations"
- Synthesis of Benzene Derivatives (2) - Polarity Reversal
- Aromatic Synthesis (3) - Sulfonyl Blocking Groups
- Birch Reduction
- Synthesis (7): Reaction Map of Benzene and Related Aromatic Compounds
- Aromatic Reactions and Synthesis Practice
- Electrophilic Aromatic Substitution Practice Problems
20 Aldehydes and Ketones
- What's The Alpha Carbon In Carbonyl Compounds?
- Nucleophilic Addition To Carbonyls
- Aldehydes and Ketones: 14 Reactions With The Same Mechanism
- Sodium Borohydride (NaBH4) Reduction of Aldehydes and Ketones
- Grignard Reagents For Addition To Aldehydes and Ketones
- Wittig Reaction
- Hydrates, Hemiacetals, and Acetals
- Imines - Properties, Formation, Reactions, and Mechanisms
- All About Enamines
- Breaking Down Carbonyl Reaction Mechanisms: Reactions of Anionic Nucleophiles (Part 2)
- Aldehydes Ketones Reaction Practice
21 Carboxylic Acid Derivatives
- Nucleophilic Acyl Substitution (With Negatively Charged Nucleophiles)
- Addition-Elimination Mechanisms With Neutral Nucleophiles (Including Acid Catalysis)
- Basic Hydrolysis of Esters - Saponification
- Transesterification
- Proton Transfer
- Fischer Esterification - Carboxylic Acid to Ester Under Acidic Conditions
- Lithium Aluminum Hydride (LiAlH4) For Reduction of Carboxylic Acid Derivatives
- LiAlH[Ot-Bu]3 For The Reduction of Acid Halides To Aldehydes
- Di-isobutyl Aluminum Hydride (DIBAL) For The Partial Reduction of Esters and Nitriles
- Amide Hydrolysis
- Thionyl Chloride (SOCl2)
- Diazomethane (CH2N2)
- Carbonyl Chemistry: Learn Six Mechanisms For the Price Of One
- Making Music With Mechanisms (PADPED)
- Carboxylic Acid Derivatives Practice Questions
22 Enols and Enolates
- Keto-Enol Tautomerism
- Enolates - Formation, Stability, and Simple Reactions
- Kinetic Versus Thermodynamic Enolates
- Aldol Addition and Condensation Reactions
- Reactions of Enols - Acid-Catalyzed Aldol, Halogenation, and Mannich Reactions
- Claisen Condensation and Dieckmann Condensation
- Decarboxylation
- The Malonic Ester and Acetoacetic Ester Synthesis
- The Michael Addition Reaction and Conjugate Addition
- The Robinson Annulation
- Haloform Reaction
- The Hell–Volhard–Zelinsky Reaction
- Enols and Enolates Practice Quizzes
23 Amines
- The Amide Functional Group: Properties, Synthesis, and Nomenclature
- Basicity of Amines And pKaH
- 5 Key Basicity Trends of Amines
- The Mesomeric Effect And Aromatic Amines
- Nucleophilicity of Amines
- Alkylation of Amines (Sucks!)
- Reductive Amination
- The Gabriel Synthesis
- Some Reactions of Azides
- The Hofmann Elimination
- The Hofmann and Curtius Rearrangements
- The Cope Elimination
- Protecting Groups for Amines - Carbamates
- The Strecker Synthesis of Amino Acids
- Introduction to Peptide Synthesis
- Reactions of Diazonium Salts: Sandmeyer and Related Reactions
- Amine Practice Questions
24 Carbohydrates
- D and L Notation For Sugars
- Pyranoses and Furanoses: Ring-Chain Tautomerism In Sugars
- What is Mutarotation?
- Reducing Sugars
- The Big Damn Post Of Carbohydrate-Related Chemistry Definitions
- The Haworth Projection
- Converting a Fischer Projection To A Haworth (And Vice Versa)
- Reactions of Sugars: Glycosylation and Protection
- The Ruff Degradation and Kiliani-Fischer Synthesis
- Isoelectric Points of Amino Acids (and How To Calculate Them)
- Carbohydrates Practice
- Amino Acid Quizzes
25 Fun and Miscellaneous
- A Gallery of Some Interesting Molecules From Nature
- Screw Organic Chemistry, I'm Just Going To Write About Cats
- On Cats, Part 1: Conformations and Configurations
- On Cats, Part 2: Cat Line Diagrams
- On Cats, Part 4: Enantiocats
- On Cats, Part 6: Stereocenters
- Organic Chemistry Is Shit
- The Organic Chemistry Behind "The Pill"
- Maybe they should call them, "Formal Wins" ?
- Why Do Organic Chemists Use Kilocalories?
- The Principle of Least Effort
- Organic Chemistry GIFS - Resonance Forms
- Reproducibility In Organic Chemistry
- What Holds The Nucleus Together?
- How Reactions Are Like Music
- Organic Chemistry and the New MCAT
26 Organic Chemistry Tips and Tricks
- Common Mistakes: Formal Charges Can Mislead
- Partial Charges Give Clues About Electron Flow
- Draw The Ugly Version First
- Organic Chemistry Study Tips: Learn the Trends
- The 8 Types of Arrows In Organic Chemistry, Explained
- Top 10 Skills To Master Before An Organic Chemistry 2 Final
- Common Mistakes with Carbonyls: Carboxylic Acids... Are Acids!
- Planning Organic Synthesis With "Reaction Maps"
- Alkene Addition Pattern #1: The "Carbocation Pathway"
- Alkene Addition Pattern #2: The "Three-Membered Ring" Pathway
- Alkene Addition Pattern #3: The "Concerted" Pathway
- Number Your Carbons!
- The 4 Major Classes of Reactions in Org 1
- How (and why) electrons flow
- Grossman's Rule
- Three Exam Tips
- A 3-Step Method For Thinking Through Synthesis Problems
- Putting It Together
- Putting Diels-Alder Products in Perspective
- The Ups and Downs of Cyclohexanes
- The Most Annoying Exceptions in Org 1 (Part 1)
- The Most Annoying Exceptions in Org 1 (Part 2)
- The Marriage May Be Bad, But the Divorce Still Costs Money
- 9 Nomenclature Conventions To Know
- Nucleophile attacks Electrophile
27 Case Studies of Successful O-Chem Students
- Success Stories: How Corina Got The The "Hard" Professor - And Got An A+ Anyway
- How Helena Aced Organic Chemistry
- From a "Drop" To B+ in Org 2 – How A Hard Working Student Turned It Around
- How Serge Aced Organic Chemistry
- Success Stories: How Zach Aced Organic Chemistry 1
- Success Stories: How Kari Went From C– to B+
- How Esther Bounced Back From a "C" To Get A's In Organic Chemistry 1 And 2
- How Tyrell Got The Highest Grade In Her Organic Chemistry Course
- This Is Why Students Use Flashcards
- Success Stories: How Stu Aced Organic Chemistry
- How John Pulled Up His Organic Chemistry Exam Grades
- Success Stories: How Nathan Aced Organic Chemistry (Without It Taking Over His Life)
- How Chris Aced Org 1 and Org 2
- Interview: How Jay Got an A+ In Organic Chemistry
- How to Do Well in Organic Chemistry: One Student's Advice
- "America's Top TA" Shares His Secrets For Teaching O-Chem
- "Organic Chemistry Is Like..." - A Few Metaphors
- How To Do Well In Organic Chemistry: Advice From A Tutor
- Guest post: "I went from being afraid of tests to actually looking forward to them".
U know…i think i study well in organic chemistry.. And when i try to do questions i almost solve every question …but when it comes to exam i think that i don’t know a single word… i just mark any random option on sheet…can u plz suggest me some tips so that i can improve this
Thnks..
The only way you are ever going to build a proper house, is by making sure the foundations are solid and well constructed. If your foundation is weak you might be able to build the house up to a storey, but then when you want to build up another storey the house collapses. Immerse yourself in reaction mechanisms, MO theory, and interpreting acidity/basicity of a compund
My son wants to eventually go to medical school and needs to do well in his organic chemistry class. I’ve never taken it, but I’ve been trying to help him through it as best as I can. I like your tip about focusing on understanding and not on memorization. He’s trying to absorb a lot of information at once and I think if he understood it all, he’d do much better on his tests. I’ll have to pass this along to him. Thanks!
My chemistry professor said organic chem does indeed require a lot of memorization.
Those tips are certainly helpfull. I past organic chemestry I and II both with 14 ( thats lik B- to B). But I want to do really good (read: better) on organic chemistry III. Here’s another tip for solving reaction problems: take a good look at reaction maps (search on google) and make reaction maps yourself. They give a good overview of possible reactions you can use.
thanks for sharing out your great piece of mind, am taking organic chemistry 1 this semester which i thought of it being tough but according to your word of advice i personally know that it would be a walk in the park by devoting myself to practicing and hard work.
thanks a lot….
thanks for sharing.While preparing the time table keep in mind that the subject you studied before must be frequently revised,revising subjects at a gap of 3 days so you will be able to decrease your efforts and will maintain a stable memory level. Remember to take regular breaks and get out and exercise. Always begin at precise time you had planned. If you would study for a continuous period, plan a few short breaks into the time.This is the way to have a valuable rest for your eyes and mind. Have a focus, do not think any distracting ideas as you are studying.
education
Just concentrate on your studies and try to stop clubbing till the end of the semester.
I am a Georgia Tech student currently in Organic Chemistry I. I’ve been doing alright so far. We have five midterms and a final exam in the class and my grades on the exams have been as follows: 95, 80, & 65. Our fourth exam was today and it was over alkene and alkyne additions. I know for a fact I did horribly on the exam…I’m thinking my score is below a 50…Thankfully, there is a drop test so it won’t count. But I’m coming here to ask how should I approach this course? I want to understand the basics so that when I take orgo 2 I won’t have as much trouble. I have a lot of extracurriculers that I do, such as working in a research lab and doing clubs, so I don’t always have a lot of time to study. Also, I’ve realized that as the semester goes on, my motivation goes down and I don’t know how to keep it up since topics start to get harder. Can someone PLEASE help me?
Hey thanks a ton!!! That was a very enlightening article on how to go about with organic!!! And yes, the mindset with which one approaches it really matters and hard work has no substitute!!
Thanks for sharing this useful information to discussed. It is simply a matter of how hard you are capable to work in order to do well. Well done.
Interesting read about a little discussed topic on chemistry blogs. It offers stimulating ideas for further discussion. Worth sharing among students.
Thanks alot, it was really helpful
well, thank you so much! I hope this proves to be effective!
Hi,
I will be taking Orgo 1 next semester, & I’m trying to figure out what to pair it with. At 12 credits, I’ll be taking Orgo 1 w/ lab, human physiology, & pre-cal, & I will also be volunteering at a hospital for 4 hours a week & tutoring for 6 hrs a week. I might also be doing research & physician shadowing, this is still pending. Should I also take neurobiology with all of these, or would that be too much?
My academic strengths lie in memorization & hard work. However, if given the right type of teacher/ tutor & practicing problems, & I can be very good in math type of courses too.
You couldn’t be more wrong about Val Kilmer in Real Genius. You’ve obviously forgotten the second study montage in which Chris Knight gets serious about his work and not only has the epiphany about synthesizing excited bromide in an argon matrix, but is able to confidently assert to Professor Hathaway that he “aced this test.” He didn’t walk into the exam unprepared; he was utterly prepared!
Thanks for giving me an excuse to re-watch the movie.
What Yannick said is very true. I got an A in org1 and org2, and I can tell you from personal experience that it requires tons and tons of practice. You will not do well in organic without doing hundreds and hundreds of problems (at least in my experience). All of the students who did well in these courses did every practice test problem they could get their hands on. It blew my mind how many of the students in the class said they were pre-med and yet they never did any practice problems; they just made flashcards and tried to memorize everything right before the test/quiz. Needless to say these are the folks who ended up with mid-50’s on the exams and probably C’s or lower for the course.
The more problems you do, the more aware you are of the mechanisms and the more engrained they become in your head. That way, come test time, it is second nature to you and it becomes a matter of regurgitating the reactions/mechanisms that you have already seen and done many, many times. As mentioned in the article, there is no magic formula. It is simply a matter of how hard you are willing to work in order to do well. Good luck.
The best way to learn and be sucessful at Organic Chemistry is practice. It is practically impossible to learn all the mechanism especially the ones in Organic Chemistry 2. You are expected to know most of them and the only way to do that is to practice by doing problems and problems, and as you are practicing, you are retaining all the mechanism for a long term without actually memorizing the mechanism only for a test. There are also an organic chemistry book called “Organic chemistry as a second language” by David klein which is one of the best Organic Chemistry book ever. You should look into that and good luck acing the class.
I thought this was a nice article. I was planning on taking an O-Chem class next year, but several threads on this topic did scare me from ever considering taking the class. I do need to work on my study habits though.
The best way of studying organic chemistry is to practice alot then memorising. Practice really helps. please could you help me with some other tips to study organic chemistry.
If you want to be an expert in chemistry, you should probably go study chemistry for the rest of your life. The more you learn, the less you will realize you understand.
I want to learn more and more basic organic chemistry. I want to become a expert in chemistry, please help me.
If you’re in AP Chemistry, please read this article with great care. It will help you improve your AP Chem grade if you necessarily need to. Our goal is to help you get an “A” and get you into the college of your choice. Whatever resource you can find, take advantage of it. It will be extremely beneficial in the long run. Again, be sure to aim high and work the problems both individually and collectively to reach your goals.
I’m glad I came across this post, its nice to know I’m not the only one struggling with Organic Chem. I just withdrew from Summer Orgo I at UNC because I was looking at a C+. I’m an older student, 29, that just came out of the military about 10 months ago and hand’t been in the civilian classroom environment in about 11 years. I found organic difficult, and I truly believe it was due to a lack of proper study habits. I say this because I literrally spent all of my out of class time reading and trying to understand the material, yet still received 70’s on the exams. I’m sitting in on the classes for the rest of the summer (including orgo II), I need to get A’s so I can bring my GPA up for med school. I feel like the material is rushed and it would greatly help other students to look at the functional groups prior to starting orgo and most importantly to develop efficient study habits. I wish I had spent more time focusing on doing the problems in the chapters instead of making sure that I read every chapter. I don’t believe any of the material is truly difficult to understand, it’s just a lot to digest in a short amount of time (in the summer anyway) Anyway, good luck to anyone that comes across these posts. Stay positive and keep your nose to the grindstone!
I’m wrapping my last quarter of ochem, I’ve got a little advice. If you want to do well in ochem make sure you learn the concepts of SN1/SN2/E1/E2 and orbital theory during in your first ochem class. These will be the theoretical concepts that apply to almost all of the chemistry your learn for the rest of the year.
As a last comment, I’m a senior wrapping up his degree. I’ve got about 15 credits after this semester (I have 117 credits). I’ve seen all kinds of teaching styles, and I would have to say organic chemistry is definitely one of the worst courses I’ve ever dealt with, due to lack of guidance on how to study.
Honestly, I think the next best thing to do is spend time with the professor and/or TA in order to get a physical understanding of what’s going on (if these things are not easily being discussed/understood). Maybe the professor is emphasizing memorization; but if that’s the case, then the trick is to spend time with that intelligent person who understands the physical aspects and actually get a grasp on the physics aspects behind all of those reactions.
I spend about 50 hours a week and still make a C. Honestly, I think there are a variety of teachings styles when it comes to organic chemistry. Professors can emphasize either the physical aspects of a reaction; otherwise, they can emphasize some kind of memorization scheme.
I think the pedagogy will depend on the mission of the university, though. For instance, I suspect a school that revolves around medical science will attempt to use a memorization pedagogy.
I’m not saying that you won’t be able to make some sense of the mechanics involved. However, I’m saying that maybe for some schools, in some universities, there is actually a lot of memorization going on.
p.s.
I study cognitive neuroscience with plenty of background in the learning sciences. I’m really good at memorizing things. And when it comes to something like the organic chemistry, however, I find that it really appears to be a large amount of memorization IF the professor does not easily allow the physical aspects of the reaction be easily understood.
You have a point. I would argue that Org 1 is different, but seeing some midterms (from pretty prestigious schools too) over the past month or so, Org 2 can definitely be tested in a way that is just a challenge of how many reactions students can regurgitate. It really does depend on the professor. The best thing you can possibly do is find a previous copy of a midterm/final to get a good handle on how they design the test.
It still helps, however, if you can see patterns and group reactions into clusters. If you didn’t get that with your prof or TA, well, you’re exactly the type of student I’d like to help.