Organic Chemistry As a Second Language: Second Semester Topics
4th Edition
ISBN: 9781119110651
Author: David R. Klein
Publisher: WILEY
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Question
Chapter 7.7, Problem 7.48P
Interpretation Introduction
Interpretation:
Efficient synthesis has to be proposed for the given transformation.
Expert Solution & Answer
Explanation of Solution
Given transformation is,
Looking into the reactant and product, it is found that the methoxy group is converted into chloride. In order to accomplish the given transformation, the ester has to be converted into
Conversion of carboxylic acid ester to carboxylic acid can be done using aqueous acid.
Carboxylic acid when treated with thionyl chloride gives acid halide as the product. This can be represented as,
Therefore, the efficient synthesis can be given as,
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Students have asked these similar questions
Deducing the reactants of a Diels-Alder reaction
n the molecule on the right-hand side of this organic reaction be made in good yield from no more than two reactants, in one
step, by moderately heating the reactants?
?
Δ
• If your answer is yes, then draw the reactant or reactants in the drawing area below. You can draw the reactants in any
arrangement you like.
• If your answer is no, check the box under the drawing area instead.
Explanation Check
Click and drag to start drawing a structure.
>
Predict the major products of the following organic reaction:
+
Some important notes:
A
?
• Draw the major product, or products, of the reaction in the drawing area below.
• If there aren't any products, because no reaction will take place, check the box below the drawing area instead.
• Be sure to use wedge and dash bonds when necessary, for example to distinguish between major products that are
enantiomers.
Explanation
Check
Click and drag to start drawing a structure.
if the answer is no reaction than state that and please hand draw!
Chapter 7 Solutions
Organic Chemistry As a Second Language: Second Semester Topics
Ch. 7.3 - Propose a plausible mechanism for each of the...Ch. 7.3 - Propose a plausible mechanism for each of the...Ch. 7.3 - Propose a plausible mechanism for each of the...Ch. 7.3 - Propose a plausible mechanism for each of the...Ch. 7.3 - Propose a plausible mechanism for each of the...Ch. 7.3 - Predict the major product in each of the following...Ch. 7.3 - Predict the major product in each of the following...Ch. 7.3 - Predict the major product in each of the following...Ch. 7.3 - Predict the major product in each of the following...Ch. 7.3 - Predict the major product in each of the following...
Ch. 7.3 - Identify the reagents you would use to achieve...Ch. 7.3 - Identify the reagents you would use to achieve...Ch. 7.3 - Identify the reagents you would use to achieve...Ch. 7.3 - Identify the reagents you would use to achieve...Ch. 7.3 - Identify the reagents you would use to achieve...Ch. 7.4 - Predict the major products for each of the...Ch. 7.4 - Predict the major products for each of the...Ch. 7.4 - Predict the major products for each of the...Ch. 7.5 - Prob. 7.23PCh. 7.5 - Identify the reagents you would use to make each...Ch. 7.5 - Identify the reagents you would use to make each...Ch. 7.5 - Identify the reagents you would use to make each...Ch. 7.5 - Identify the reagents you would use to make each...Ch. 7.5 - In the space provided, draw a mechanism for each...Ch. 7.5 - In the space provided, draw a mechanism for each...Ch. 7.5 - Prob. 7.33PCh. 7.5 - Prob. 7.34PCh. 7.5 - Prob. 7.35PCh. 7.5 - Prob. 7.36PCh. 7.6 - Based on everything we have just seen, propose a...Ch. 7.6 - Prob. 7.39PCh. 7.6 - Prob. 7.40PCh. 7.6 - Prob. 7.41PCh. 7.6 - Propose a mechanism for the following reaction:Ch. 7.6 - Prob. 7.44PCh. 7.6 - Prob. 7.45PCh. 7.6 - Prob. 7.46PCh. 7.7 - Prob. 7.48PCh. 7.7 - Prob. 7.49PCh. 7.7 - Prob. 7.50PCh. 7.7 - Prob. 7.51PCh. 7.7 - Prob. 7.52PCh. 7.7 - Prob. 7.53PCh. 7.7 - Prob. 7.55PCh. 7.7 - Prob. 7.56PCh. 7.7 - Prob. 7.57PCh. 7.7 - Prob. 7.58PCh. 7.7 - Prob. 7.59PCh. 7.7 - Prob. 7.60PCh. 7.7 - Prob. 7.61PCh. 7.7 - Prob. 7.62PCh. 7.7 - Prob. 7.63PCh. 7.7 - Prob. 7.64PCh. 7.7 - Prob. 7.65P
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