CH3 HCI

Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Draw the major product(s) of the following reaction.

The image depicts a chemical reaction. 

On the left side is a chemical structure: a six-membered carbon ring (cyclohexane) with a single double bond connecting to a carbon chain ending with a methyl group (CH₃), which indicates a type of alkene. 

An arrow points to the right, indicating the direction of the reaction. Above the arrow is HCl, showing that hydrochloric acid is the reagent used in the reaction. 

This setup suggests that the reaction involves an alkene undergoing an addition reaction with hydrochloric acid, likely forming a haloalkane as the product.
Transcribed Image Text:The image depicts a chemical reaction. On the left side is a chemical structure: a six-membered carbon ring (cyclohexane) with a single double bond connecting to a carbon chain ending with a methyl group (CH₃), which indicates a type of alkene. An arrow points to the right, indicating the direction of the reaction. Above the arrow is HCl, showing that hydrochloric acid is the reagent used in the reaction. This setup suggests that the reaction involves an alkene undergoing an addition reaction with hydrochloric acid, likely forming a haloalkane as the product.
Expert Solution
Step 1: Protonation of Double Bond

A double bond is protonated by an acid to produce the most stable carbocation as the major intermediate. The most stable carbocation is identified by the most number of hyperconjugative atoms present in it.

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