Essential Organic Chemistry (3rd Edition)
Essential Organic Chemistry (3rd Edition)
3rd Edition
ISBN: 9780321937711
Author: Paula Yurkanis Bruice
Publisher: PEARSON
Question
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Chapter 18, Problem 32P
Interpretation Introduction

Interpretation:

Compound that can remove HBr more rapidly in a basic solution has to be identified.

Concept introduction:

  • Catalyst: Substance which helps in increasing the rate of a particular reaction without getting consumed in the reaction.
  • Base Catalyst: A catalyst which helps in increasing the rate of a particular reaction by the removal of a proton. There are two types of catalysis:
  1. 1. Specific-base catalysis: Proton is completely removed before the slow step in a reaction
  2. 2. General- base catalysis: Proton is completely removed during the slow step in a reaction
  • Intramolecular general-base catalysis: A catalysis where catalyst is a part of the molecule that undergoes the reaction promotes the reaction in a species by completely removing a proton during the slow step in a reaction

Expert Solution & Answer
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Explanation of Solution

In the below compound, negatively charged oxygen atom is in axial position where it can easily undergo intramolecular general-base reaction comparing to O group in equatorial position. Here, the O act as the intramolecular catalyst where it attacks the proton atom from the carbon atom that is attached to CH2Br group. Thus, HBr is easily removed in the below compound due to the position of negatively charge oxygen.

  Essential Organic Chemistry (3rd Edition), Chapter 18, Problem 32P , additional homework tip  1

Therefore, the compound where HBr is easily removed in a basic solution is,

  Essential Organic Chemistry (3rd Edition), Chapter 18, Problem 32P , additional homework tip  2

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Chapter 18 Solutions

Essential Organic Chemistry (3rd Edition)

Ch. 18.7 - Prob. 11PCh. 18.8 - How many conjugated double bonds are there in a....Ch. 18.8 - Instead of adding to the 4a-position and...Ch. 18.8 - In succinate dehydrogenase, FAD is covalently...Ch. 18.8 - Prob. 15PCh. 18.9 - Acetolactate synthase is another TPP-requiring...Ch. 18.9 - Acetolactate synthase can also transfer the acyl...Ch. 18.9 - Prob. 18PCh. 18.9 - Prob. 19PCh. 18.10 - Prob. 21PCh. 18.11 - Prob. 23PCh. 18.11 - Which compound is more easily decarboxylated?Ch. 18.11 - Explain why the ability of PLP to catalyze an...Ch. 18.11 - Explain why the ability of PLP to catalyze an...Ch. 18.12 - What groups are interchanged in the following...Ch. 18.13 - Why is the coenzyme called tetrahydrofolate?Ch. 18.13 - What amino acid is formed by the following...Ch. 18.13 - How do the structures of tetrahydrofolate and...Ch. 18.13 - What is the source of the methyl group in...Ch. 18 - Prob. 32PCh. 18 - Prob. 33PCh. 18 - From what vitamins are the following coenzymes...Ch. 18 - Prob. 35PCh. 18 - For each of the following reaction, name both the...Ch. 18 - Explain why serine proteases do not catalyze...Ch. 18 - Prob. 38PCh. 18 - For each of the following enzyme catalyzed...Ch. 18 - Trisephosphate isomerase (TIM) catalyzes the...Ch. 18 - Prob. 41PCh. 18 - What acyl groups have we seen transferred by...Ch. 18 - When UMP is dissolved in T2O, exchange of T for H...Ch. 18 - Prob. 44PCh. 18 - When transaminated, the three branched-chain amino...Ch. 18 - Aldolase shows no activity if it is incubated with...
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