Consider the acid-catalyzed hydration of 3-methyl-1-butene. For each of the four steps, add one or two curved arrows to the Learning reactant side to show the mechanism. Do not delete any pre-drawn bonds, charges, or lone pairs. Remove the last change by using the undo button on the lower left or revert the drawing palette to the original state by selecting the More menu, then select Reset Drawing. Step 1 H CH, CH2 - H3C-C-C+ H. H. ČH3 H. сн, н

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Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
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Step 3
H.
H
H3C-C-CH2-CH3
ČH3
H,C
Step 4
H.
- |-
H.
:-
H.
H3C-C-CH2-CH3
CH,
H,C - C
ČH3
CH,
Transcribed Image Text:Step 3 H. H H3C-C-CH2-CH3 ČH3 H,C Step 4 H. - |- H. :- H. H3C-C-CH2-CH3 CH, H,C - C ČH3 CH,
Loudon| Panse SEVENTH EDITION
presented by Macmillan Learning
Consider the acid-catalyzed hydration of 3-methyl-1-butene. For each of the four steps, add one or two curved arrows to the
reactant side to show the mechanism.
Do not delete any pre-drawn bonds, charges, or lone pairs. Remove the last change by using the undo button on the lower left
or revert the drawing palette to the original state by selecting the More menu, then select Reset Drawing.
Step 1
H.
H
CH2
CH,
H,C
H3C-
-C+
H
CH3
CH,
Step 2
CH3
CH,
H3C-c
-H-
H,C - C
H.
ČH3
H.
CH,
Transcribed Image Text:Loudon| Panse SEVENTH EDITION presented by Macmillan Learning Consider the acid-catalyzed hydration of 3-methyl-1-butene. For each of the four steps, add one or two curved arrows to the reactant side to show the mechanism. Do not delete any pre-drawn bonds, charges, or lone pairs. Remove the last change by using the undo button on the lower left or revert the drawing palette to the original state by selecting the More menu, then select Reset Drawing. Step 1 H. H CH2 CH, H,C H3C- -C+ H CH3 CH, Step 2 CH3 CH, H3C-c -H- H,C - C H. ČH3 H. CH,
Expert Solution
Step 1

The reaction in which alkene is converted into alcohol by the addition of a water molecule is called a hydration reaction. The reaction is driven by the carbocation formation, hydride shift, and oxonium formation. In this reaction, the more substituted product is the major product. It follows Markovnikoff's rule.

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