5. For each reaction: i) determine the type of haloalkane (primary, secondary, etc.); ii) determine the nature of the base/nucleophile; predict whether the reaction is SN1, SN2, E1, or E2; iii) draw the structures of the intermediate/transition states: iv) and then, the most favorable product(s) of the following reactions. Br C a) C-c-d-c + On > C-c--c-8, + I→ b)

Chemistry
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ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
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Chapter1: Chemical Foundations
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5. For each reaction: i) determine the type of haloalkane (primary, secondary, etc.); ii) determine the
nature of the base/nucleophile; predict whether the reaction is SN1, SN2, E1, or E2; iii) draw the structures
of the intermediate/transition states: iv) and then, the most favorable product(s) of the following reactions.
Br C
a) c-d-è-c + on >
b)
Transcribed Image Text:5. For each reaction: i) determine the type of haloalkane (primary, secondary, etc.); ii) determine the nature of the base/nucleophile; predict whether the reaction is SN1, SN2, E1, or E2; iii) draw the structures of the intermediate/transition states: iv) and then, the most favorable product(s) of the following reactions. Br C a) c-d-è-c + on > b)
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