ORGANIC CHEMISTRY II LAB MANUAL>CUSTOM<
ORGANIC CHEMISTRY II LAB MANUAL>CUSTOM<
9th Edition
ISBN: 9780534261641
Author: SIMEK
Publisher: Cengage Learning
Question
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Chapter 21, Problem 21.62SP

(a)

Interpretation Introduction

Interpretation:

An equation for the reaction that took place in the tank of methyl isocyanate with water (Bhopal gas accident) and an explanation for the rose in pressure and temperature dramatically are to be stated.

Concept introduction:

At 25°C, methyl isocyanate is a volatile liquid, has a low boiling point (39.5°C) and has a high vapour pressure (57.7kPa). It is highly toxic in nature that irritate throat and nose.

(b)

Interpretation Introduction

Interpretation:

A mechanism for the reaction that took place in the tank of methyl isocyanate with water in the Bhopal gas accident is to be stated.

Concept introduction:

A mechanism of the reaction between methyl isocyanate and water comprises two steps. The first step is nucleophilic attack of water molecule on the carbonyl carbon followed by formation of an acid. The second step is cleavage of the bond between carbonyl carbon and nitrogen by deprotonation of acid and protonation of amine (exchange of proton).

(c)

Interpretation Introduction

Interpretation:

An alternative synthesis of Sevin is to be stated.

Concept introduction:

Diethyl carbonate is an ester (prepared from carbonic acid and ethanol). It is a liquid reagent that is easy to handle. However, phosgene is a corrosive and highly toxic. Diethyl carbonate successfully replaces phosgene in the synthesis of Lexan and Sevin.

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Chapter 21 Solutions

ORGANIC CHEMISTRY II LAB MANUAL>CUSTOM<

Ch. 21.7C - Prob. 21.20PCh. 21.7C - Prob. 21.21PCh. 21.7D - Prob. 21.22PCh. 21.7D - The mechanism for acidic hydrolysis of a nitrile...Ch. 21.8A - Prob. 21.24PCh. 21.8C - Prob. 21.25PCh. 21.9 - Prob. 21.26PCh. 21.9 - Prob. 21.27PCh. 21.9 - Prob. 21.28PCh. 21.10 - Draw a mechanism for the acylation of anisole by...Ch. 21.10 - Prob. 21.30PCh. 21.11 - Prob. 21.31PCh. 21.11 - Prob. 21.32PCh. 21.12 - Problem 21-33 Propose a mechanism for the...Ch. 21.12 - Suggest the most appropriate reagent for each...Ch. 21.12 - Show how you would synthesize each compound,...Ch. 21.13 - Prob. 21.36PCh. 21.13 - Prob. 21.37PCh. 21.14 - Prob. 21.38PCh. 21.14 - Prob. 21.39PCh. 21.16 - Prob. 21.40PCh. 21.16 - Prob. 21.41PCh. 21 - Prob. 21.42SPCh. 21 - Give appropriate names for the following...Ch. 21 - Predict the major products formed when benzoyl...Ch. 21 - Predict the products of the following reactions....Ch. 21 - Prob. 21.46SPCh. 21 - Prob. 21.47SPCh. 21 - Prob. 21.48SPCh. 21 - Propose mechanisms for the following reactions.Ch. 21 - Prob. 21.51SPCh. 21 - An ether extraction of nutmeg gives large...Ch. 21 - Prob. 21.53SPCh. 21 - Show how you would accomplish the following...Ch. 21 - Prob. 21.55SPCh. 21 - Prob. 21.56SPCh. 21 - Prob. 21.57SPCh. 21 - Prob. 21.58SPCh. 21 - Prob. 21.59SPCh. 21 - Explain this curious result. What does this...Ch. 21 - Prob. 21.61SPCh. 21 - Prob. 21.62SPCh. 21 - Prob. 21.63SPCh. 21 - A chemist was called to an abandoned aspirin...Ch. 21 - Prob. 21.67SPCh. 21 - The IR spectrum, 13ONTVTR spectrum, and 1HNMR...Ch. 21 - Prob. 21.69SPCh. 21 - Prob. 21.70SPCh. 21 - Prob. 21.71SP
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