Comments on: Organic Chemistry Study Tips: Learn the Trends https://www.masterorganicchemistry.com/2010/04/09/organic-chemistry-study-tips-learn-the-trends/ Tue, 23 Jan 2024 21:15:11 +0000 hourly 1 https://wordpress.org/?v=6.6.2 By: Best Chemistry Apps for Android and Iphone - Learn Chemistry Easily https://www.masterorganicchemistry.com/2010/04/09/organic-chemistry-study-tips-learn-the-trends/#comment-565268 Thu, 26 Sep 2019 15:04:27 +0000 http://masterorganicchemistry.wordpress.com/?p=216#comment-565268 […] topic is the most difficult one in the subject the majority of them will answer that it is the Organic chemistry. It is tedious to remember all the structures, formulas and reactions in organic chemistry. For […]

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By: James Ashenhurst https://www.masterorganicchemistry.com/2010/04/09/organic-chemistry-study-tips-learn-the-trends/#comment-554702 Fri, 03 May 2019 19:13:32 +0000 http://masterorganicchemistry.wordpress.com/?p=216#comment-554702 In reply to Luca Shanley.

The higher the pKa the weaker the acid. The weaker the acid, the stronger (more unstable) the conjugate base. So yes, you are correct.

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By: Luca Shanley https://www.masterorganicchemistry.com/2010/04/09/organic-chemistry-study-tips-learn-the-trends/#comment-541257 Wed, 24 Oct 2018 21:28:06 +0000 http://masterorganicchemistry.wordpress.com/?p=216#comment-541257 As you increase the pKa of an acid wouldn’t that decrease the stability of the base?

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By: Ningxin https://www.masterorganicchemistry.com/2010/04/09/organic-chemistry-study-tips-learn-the-trends/#comment-530452 Tue, 03 Apr 2018 18:21:35 +0000 http://masterorganicchemistry.wordpress.com/?p=216#comment-530452 Hi!
Just wanted to thank you for all your wonderful help on organic chemistry! I’d be so lost without your site. Your cheat sheets are so detailed and helpful! I love the formatting; it’s all so clear and easy to understand. Thanks again and hope you have a great day!

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By: Kaustubh https://www.masterorganicchemistry.com/2010/04/09/organic-chemistry-study-tips-learn-the-trends/#comment-358618 Fri, 30 Jan 2015 10:25:30 +0000 http://masterorganicchemistry.wordpress.com/?p=216#comment-358618 Can u tell me about the stability of carbonium ions a little more.
I.e cyclo propyl group attached car cat ion is more stable than any thing else . why is it so… and little info about some carbonium ions having benzyl group and some more groups attached to it , such as NH2 …

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By: Zuala Jongte https://www.masterorganicchemistry.com/2010/04/09/organic-chemistry-study-tips-learn-the-trends/#comment-90436 Wed, 30 Apr 2014 05:37:21 +0000 http://masterorganicchemistry.wordpress.com/?p=216#comment-90436 Thank you. I am so gratefull to have found your site. I have improved a lot.

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By: Nima Omid-Fard https://www.masterorganicchemistry.com/2010/04/09/organic-chemistry-study-tips-learn-the-trends/#comment-2642 Tue, 13 Mar 2012 04:32:56 +0000 http://masterorganicchemistry.wordpress.com/?p=216#comment-2642 In reply to james.

O right, I mistakenly thought S-character meant “single bond” character. thanks!

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By: james https://www.masterorganicchemistry.com/2010/04/09/organic-chemistry-study-tips-learn-the-trends/#comment-2606 Mon, 12 Mar 2012 00:16:59 +0000 http://masterorganicchemistry.wordpress.com/?p=216#comment-2606 In reply to Nima Omid-Fard.

Alkynes are sp hybridized (50% s character) and are more acidic C-H bonds. Alkanes are sp3 hybridized (25% S character) and are less acidic.

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By: Nima Omid-Fard https://www.masterorganicchemistry.com/2010/04/09/organic-chemistry-study-tips-learn-the-trends/#comment-2591 Sat, 10 Mar 2012 21:30:25 +0000 http://masterorganicchemistry.wordpress.com/?p=216#comment-2591 Doesn’t increasing the S-character of a bond decrease acidity of the bond? I.e C-H bond is less acidic than C(triple bond)H?? This little summary sheet says opposite?

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By: jaspreet kaur https://www.masterorganicchemistry.com/2010/04/09/organic-chemistry-study-tips-learn-the-trends/#comment-2175 Thu, 09 Feb 2012 10:49:37 +0000 http://masterorganicchemistry.wordpress.com/?p=216#comment-2175 gud to see such type of website.thanks to u .

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