1. Which are the factors that favor SN2 reactions, as described during the lab lecture? a) Strong nucleophile, good leaving group, polar protic solvent, methyl or primary halide. b) Strong nucleophile, good leaving group, polar aprotic solvent, methyl or primary halide. c) Weak nucleophile, good leaving group, polar aprotic solvent, methyl or primary halide. d) Strong nucleophile, poor leaving group, polar aprotic solvent, tertiary halide. e) Strong nucleophile, good leaving group, polar aprotic solvent, tertiary halide.

Organic Chemistry: A Guided Inquiry
2nd Edition
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Andrei Straumanis
Chapter14: Elimination
Section: Chapter Questions
Problem 32CTQ
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1. Which are the factors that favor SN2 reactions, as described during the lab lecture?
a) Strong nucleophile, good leaving group, polar protic solvent, methyl or primary halide.
b) Strong nucleophile, good leaving group, polar aprotic solvent, methyl or primary halide.
Weak nucleophile, good leaving group, polar aprotic solvent, methyl or primary halide.
d) Strong nucleophile, poor leaving group, polar aprotic solvent, tertiary halide.
e) Strong nucleophile, good leaving group, polar aprotic solvent, tertiary halide.
2. Which alkyl halide reacts fastest with trimethylamine in SN2 reaction?
D) / P
Br
b)
4₁
S
d)
) Le
Transcribed Image Text:1. Which are the factors that favor SN2 reactions, as described during the lab lecture? a) Strong nucleophile, good leaving group, polar protic solvent, methyl or primary halide. b) Strong nucleophile, good leaving group, polar aprotic solvent, methyl or primary halide. Weak nucleophile, good leaving group, polar aprotic solvent, methyl or primary halide. d) Strong nucleophile, poor leaving group, polar aprotic solvent, tertiary halide. e) Strong nucleophile, good leaving group, polar aprotic solvent, tertiary halide. 2. Which alkyl halide reacts fastest with trimethylamine in SN2 reaction? D) / P Br b) 4₁ S d) ) Le
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