Home / Why Do Organic Chemists Use Kilocalories?
Fun and Miscellaneous
Why Do Organic Chemists Use Kilocalories?
Last updated: May 24th, 2021 |
What’s the deal with organic chemists using kilocalories (kcal) instead of kilojoules (kJ)?
The metric system, of System Internationale (SI) was first adopted in France in 1791 soon after the French Revolution (one of their other innovations adopted by the revolutionaries – the ten-day week – did not survive). I’m Canadian, so I grew up entirely within the metric system, and since SI units are the de rigueur of measurement in science, I just assumed that all scientists used it.
When I started hanging out with organic chemists it was like finding acoven of shameless heretics operating right under the noses of the Inquisition. All the values of the bond strengths and energies that I’d learned and memorized in kilojoules/mol were being thrown back at me in kilocalories. Being Canadian (and a new grad student) I politely held back my criticism of this barbaric practice until a more opportune time, while simultaneously maintaining my smugness that SI was the more correct system.
[Just to jog your memory, a “calorie” is a unit of energy measurement. It’s the energy required to raise the temperature of 1 gram of water by 1 degree Celsius. Although it’s still used as a unit of food energy, the calorie has been replaced by the Systeme Internationale unit the joule (J). A calorie is equal to 4.184 J. ]
After a few weeks of hearing my colleagues banter in kilocalories, it started to dawn on me that it wasn’t just my own research group that did this. It was the whole community of organic chemists – in journals, at conferences, in casual conversation. And little by little, I started using it too. It felt kind of naughty at first to get away from my Systeme Internationale upbringing. Month by month, however, my resistance to using kcals started crumbling – the more I used it, the more I realized it was actually a more practical unit of measurement for organic chemistry.
In Gen chem we learn how to look up the heats of formation of whole molecules, which can be pretty big numbers. In contrast, when organic chemists talk about energies, they are usually talking about bond dissociation energies and conformations. Since the variety of molecules in organic chemistry is so huge, we often don’t have the luxury of being able to work with values from tables. Therefore, when thinking about the energy changes in a reaction, we’re often forced to base our reasoning on estimating the value of the parts rather than the whole. “What’s that C-O bond worth? What does it cost to replace it with bromide? What’s the energy for that ring flip? What’s the contribution of that hydrogen bond?”.
It’s kind of like going from working at a car dealership to a chop shop and one day finding yourself looking at a car and thinking “what’s that bumper worth?”
So why do organic chemists use kcals? I can think of 4 reasons.
1. The C-H bond strength in alkanes of 100 kcal/mol is a convenient mental anchor.
Organic chemists think a lot in terms of bond strengths. The most common bond you’ll find in organic chemistry is the C-H bond, which has a bond strength of about 100 kcal/mol (note: this value can vary considerably depending on the substitution at carbon, but for simple alkanes like methane and ethane, the C-H bond is very close to this value). What’s that value in kJ/mol? 472 kJ/mol. Guess which number is easier to remember?
There’s just something instinctive about working on a 0-100 scale.
2. Low-energy phenomena also fit well on the kcal scale too.
For organic chemistry, kcal/mol is kind of a “goldilocks” metric in that even 1 kcal/mol is significant, but not too significant. For instance, 1 kcal/mol is not even close to being enough energy to break a bond, but it’s still enough to cause an 83:17 ratio of products at equilibrium. Going a little bit higher, hydrogen bonds have strengths of anywhere from 2-7 kcal/mol.
Along the same lines, when you learn about conformations you are told that the barrier to rotation of ethane (from the “eclipsed” to the “staggered” form)is about 10 kJ/mol. Converted into kcal, that’s about 2.8 kcal/mol.
So on one end you have the strength of the C-H bond at 100 and on the other end you have hydrogen bonds and conformational changes from around 2-7 kcal/mol. The scale incorporates them both very well.
3. In general, smaller numbers are easier to deal with.
One thing about bond strength values that you’ll see is that they vary a lot. Depending on where you look you might see values of 78-82 kcal/mol for the C-C bond strength. Dealing with an uncertainty of 4 seems a lot easier than the equivalent with kJ, which would be 320-340 kJ/mol. Maybe it’s just me, but I like dealing with smaller numbers. As one commenter said when I asked Chemistry Reddit about this a few days ago, “kcals make my errors look smaller.”
4. When they can, organic chemists like to stick it to the French.
Just kidding. Actually, according to Wikipedia, the metric system was developed in England and introduced to France by Benjamin Franklin. Is there anything Ben Franklin wasn’t involved in? That guy was amazing.
Bottom line: Organic chemists find kcal/mol to be much more convenient to use as energy units. Personally, I think and talk in kcal/mol but because I don’t want to increase the confusion that people already feel about organic chemistry, so I try to keep things in kJ/mol here, but if I lapse back into the energy measurement I find most comfortable to work with, this is why.
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".
Very good post. I certainly appreciate this website.
Continue the good work!
Wow. You make a living by being passionate about the metric system. That’s amazing.
If it’s any consolation the chance of organic chemists moving to barrel-oil-equivalents for bond strengths is pretty low.
I suppose that you can measure energy in joules or you can use one or other of the alternatives.
Here are some that I have collected in the last 12 months.
Atomic energy unit, barrel oil equivalent, bboe, billion electron volts, Board of Trade unit, BOE, BOT, brake horsepower-hour, British thermal unit, British thermal unit (16 °C), British thermal unit (4 °C), British thermal unit (international), British thermal unit (ISO), British thermal unit (IT), British thermal unit (mean), British thermal unit (thermal), British thermal unit (thermochemical), British thermal unit-39, British thermal unit-59, British thermal unit-60, British thermal unit-IT, British thermal unit-mean, British thermal unit-th, BThU, BThU-39, BThU-59, BThU-60, BThU-IT, BThU-mean, BThU-th, Btu, Btu-39, Btu-59, Btu-60, Btu-IT, Btu-mean, Btu-th, cal, cal-15, cal-20, cal-mean, calorie, Calorie, calorie (16 °C), calorie (20 °C), calorie (4 °C), calorie (diet kilocalorie), calorie (int.), calorie (IT) (International Steam Table), calorie (mean), calorie (thermochemical), calorie-15, Calorie-15, calorie-20, Calorie-20, calorie-IT, Calorie-IT, calorie-mean, Calorie-mean, calorie-th, Calorie-th, cal-th, Celsius heat unit, Celsius heat unit (int.), Celsius heat unit-IT, Celsius heat unit-mean, Celsius heat unit-th, centigrade heat unit, centigrade heat unit-mean, centigrade heat unit-th, Chu, Chu-IT, Chu-mean, Chu-th, coulomb volt, cubic centimetre atmospheres, cubic foot atmospheres, cubic metre atmospheres, double Rydberg, duty, dutys, dyne centimetres, E-h, electron mass energy equivalent, electron volt, equivalent volt, erg, eV, foot grains, foot pound, foot pound force, foot poundal, ft-lb, ft-lbf, ft-pdl, gigaelectronvolt, gram calorie, gram calorie-15, gram calorie-20, gram calorie-IT, gram calorie-mean, gram calories (mean), gram calorie-th, grand calorie, grand calorie-15, grand calorie-20, grand calorie-IT, grand calorie-mean, grand calorie-th, hartree, Hartree energy, horsepower hours, horsepower hours (metric), inch pound force, Kayser, kcal, kcal-15, kcal-20, kcal-mean, kcal-th, kgfm, kilocalorie, kilocalorie (16 °C), kilocalorie (4 °C), kilocalorie (int.), kilocalorie-15, kilocalorie-20, kilocalorie-IT, kilocalorie-mean, kilocalorie-th, kiloelectronvolt, kilogram calorie, kilogram calorie-15, kilogram calorie-20, kilogram calorie-IT, kilogram calorie-mean, kilogram calories (int.), kilogram calorie-th, kilogram force metre, kiloton TNT equivalent, kilowatt hour, kilowatt minute, kilowatt second, kWh, large calorie, large calorie-15, large calorie-20, large calorie-IT, large calorie (mean), large calorie-th, Latm, latm, litre atmosphere, major calorie, major calorie-15, major calorie-20, major calorie-IT, major calorie-mean, major calorie-th, megaelectronvolt, megaton TNT equivalent, megawatt hours, metric ton oil, metric ton TNT, metric ton coal, micri-erg, natural unit of energy, newton metre, petit calorie, petit calorie-15, petit calorie-20, petit calorie-IT, petit calorie-mean, petit calorie-th, Q unit, quad, quadrillion, Rydberg, small calorie, small calorie-15, small calorie-20, small calorie-IT, small calorie-mean, small calorie-th, therm, therm (EC), therm (EU), therm (UK), therm (US), thermie (16 °C), ton coal equivalent, ton oil equivalent, ton TNT equivalent, tonne coal equivalent, tonne oil equivalent, tonne TNT equivalent, watt hour, watt minute, and watt second.
Conversion factors needed for 199 names = 39 402
Notice all the different BTUs, BThU, btus, calories, Calories, Cals, and cals as these all have different values according to the temperature that the observations were made.
Also note the near impossibility of our politicians rationally discussing energy in the context of peak oil, peak energy, global warming, or climate change given the confusion and obfuscation possible with all of these units.
On the other hand, if we use joules for energy in all contexts, there is only one value and only one definition, and the only conversion is to decife on whether to use millijoules, joules, kilojoules, and so on.
Cheers,
Pat Naughtin
Geelong, Australia
I like that perspective – units are a means to an end.
Another thing to realize is that they’re essential for communication between disciplines. There is no end to the confusion that can be created by not using units, something a lot of engineers I work around are prone to do.
Thanks for explaining this. As a physicist, I too was reared with the notion that to deviate from SI was a sin. I recall being upset when people would express particle energies in MeV or keV.
What’s interesting is that, in my current field, we talk about particle energies a lot, and I’ve finally become accustomed to using these units and see the utility in adapting the system to serve your needs. If someone walked up to me and started talking 8 femtojoule protons, I’d probably look at them as if they were from Mars….50 MeV, though, that’s alright.
Thanks for explaining this to me – our class just got into conformations this past week and I see now why expressing energies in kcal/mol is useful, now that I’m looking at a ring or chain and trying to figure out what the change in the Gibbs energy is from one conformer to another. Thanks James.
MSO
My pleasure, glad you found it useful.
The classes I’ve seen seem to vary about 50:50 on whether kcal or kJ are used. I think sometimes we forget that the units exist to serve us, not the other way around. I’m all for consistency but if there is a significant advantage in understanding to gained by using a slightly different metric, by all means go for it.