Questions labelled with an * are of exam standard. Substitution reactions *Qu 1. Draw the mechanism for the following reactions - first is it SN1 or SN2? (a) H₂C -Br SN2 type reaction mechanism. (b) of SN1 type reaction mechanism. (c) H₂C -Br SN2 type reaction mechanism. (c) generation of a planar carbocation generation of a planar carbocation SN1 type reaction mechanism. Qu 2. Draw the accompanying reaction coordinate diagrams (energy profile of the reaction) for the reactions in 5(a) and 5(b). DELL *Qu 7. Predict the product and give the stereochemistry of reactions of the following nucleophiles with (R)-2-bromobutane (a) CN- (b) CH3CO2 H3C H H CH3 CN -Br NC CH3CH2 R S H2CH3C H H H3C CH3CO₂ CH3 -Br CH3COO CH3CH 2 R S H2CH3C
Questions labelled with an * are of exam standard. Substitution reactions *Qu 1. Draw the mechanism for the following reactions - first is it SN1 or SN2? (a) H₂C -Br SN2 type reaction mechanism. (b) of SN1 type reaction mechanism. (c) H₂C -Br SN2 type reaction mechanism. (c) generation of a planar carbocation generation of a planar carbocation SN1 type reaction mechanism. Qu 2. Draw the accompanying reaction coordinate diagrams (energy profile of the reaction) for the reactions in 5(a) and 5(b). DELL *Qu 7. Predict the product and give the stereochemistry of reactions of the following nucleophiles with (R)-2-bromobutane (a) CN- (b) CH3CO2 H3C H H CH3 CN -Br NC CH3CH2 R S H2CH3C H H H3C CH3CO₂ CH3 -Br CH3COO CH3CH 2 R S H2CH3C
Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter19: Eas: Electrophilic Aromatic Substitution
Section: Chapter Questions
Problem 45E
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I cannot understand why the directions have been changed
Why does a is a Sn2 even thought it is a tertiary carbons?
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