For problem 8.17, all of the reactions will be SN2. For each reaction, identify and evaluate each nucleophile (strong? weak? Strong or weak as a base?) Also, evaluate each solvent as polar protic or polar aprotic. I recommend drawing the structure of each solvent. PROBLEMS8.17 Write the structure of the principal organic product to be expected from the reaction of1-bromopropane with each of the following:(a) Sodium iodide in acetone0(b) Sodium acetate (CH₂CONa) in acetic acid(c) Sodium ethoxide in ethanol(d) Sodium cyanide in dimethyl sulfoxide(e) Sodium azide in aqueous ethanol(f) Sodium hydrogen sulfide in ethanol(g) Sodium methanethiolate (NaSCH,) in ethanol

AS PER ANSWERING GUIDELINES,I WILL ANSWER ONLY FIRST THREE PART.

Answered: PROBLEMS 8.17 Write the structure of…

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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For problem 8.17, all of the reactions will be SN2. For each reaction, identify and evaluate each nucleophile (strong? weak? Strong or weak as a base?) Also, evaluate each solvent as polar protic or polar aprotic. I recommend drawing the structure of each solvent.

PROBLEMS
8.17 Write the structure of the principal organic product to be expected from the reaction of
1-bromopropane with each of the following:
(a) Sodium iodide in acetone
0
(b) Sodium acetate (CH₂CONa) in acetic acid
(c) Sodium ethoxide in ethanol
(d) Sodium cyanide in dimethyl sulfoxide
(e) Sodium azide in aqueous ethanol
(f) Sodium hydrogen sulfide in ethanol
(g) Sodium methanethiolate (NaSCH,) in ethanol

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