ORGANIC CHEM PRINT STUDY GDE & SSM
ORGANIC CHEM PRINT STUDY GDE & SSM
4th Edition
ISBN: 9781119810650
Author: Klein
Publisher: WILEY
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Chapter 3, Problem 75IP
Interpretation Introduction

Interpretation:

The drastic change in pka -value of amines in the presence of cyano group is needed to be explained and the more acidic ( pka lower than 17) amines attached by a R group is needed to find out.

Concept introduction:

pka -value of compound gives the strength of acidity of a compound. The lesser the value of pka will have more acidic strength. Stability of conjugate base determines the strength of acid.

The conjugate base having resonance will have greater stability as compared to conjugate base having single anion. Because of the resonance, conjugate base will get resonance stabilization.

To Explain: the drastic change in pka -values of amines in presence of the cyano group.

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I have a question about this problem involving mechanisms and drawing curved arrows for acids and bases. I know we need to identify the nucleophile and electrophile, but are there different types of reactions? For instance, what about Grignard reagents and other types that I might not be familiar with? Can you help me with this? I want to identify the names of the mechanisms for problems 1-14, such as Gilman reagents and others. Are they all the same? Also, could you rewrite it so I can better understand? The handwriting is pretty cluttered. Additionally, I need to label the nucleophile and electrophile, but my main concern is whether those reactions differ, like the "Brønsted-Lowry acid-base mechanism, Lewis acid-base mechanism, acid-catalyzed mechanisms, acid-catalyzed reactions, base-catalyzed reactions, nucleophilic substitution mechanisms (SN1 and SN2), elimination reactions (E1 and E2), organometallic mechanisms, and so forth."
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