Organic Chemistry (8th Edition)
Organic Chemistry (8th Edition)
8th Edition
ISBN: 9780134042282
Author: Paula Yurkanis Bruice
Publisher: PEARSON
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Chapter 11.1, Problem 1P
Interpretation Introduction

Interpretation:

From the given set of reactions the reactions those favor the formation of products have to be identified.

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Draw an energy diagram for the Brønsted–Lowry acid–base reaction of CH3CO2H with −OC(CH3)3 to form CH3CO2− and (CH3)3COH. Label the axes, starting materials, products, ΔH°, and Ea. Draw the structure of the transition state.
For the following reaction, K> 1. Classify each of the reactants and products based on their strength as Bronsted-Lowry acids or bases. CH3COOH + C18H2103NC18H2103NH+ + CH3COO- C18H2103NH+ CH3COO C18H2103N CH3COOH 1) Stronger Bronsted-Lowry acid 2) Weaker Bronsted-Lowry acid 3) Stronger Bronsted-Lowry base 4) Weaker Bronsted-Lowry base
NaHCO3 can deprotonate benzoic acid but cannot deprotonate phenol. On the other hand, NaOH can deprotonate both benzoic acid and phenol. Given this information, rank the molecules numbered I to V in order of decreasing acidity. COH cOH он H,0 H,CO, IV CH3 II I II (A) V > II >I > III > IV (В) II > 1 > V > III IV (C) II > V >I > IV > II

Chapter 11 Solutions

Organic Chemistry (8th Edition)

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