ORGANIC CHEMISTRY (LOOSELEAF)-PACKAGE
ORGANIC CHEMISTRY (LOOSELEAF)-PACKAGE
10th Edition
ISBN: 9781260008562
Author: Carey
Publisher: MCG
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Chapter 17.16, Problem 19P
Interpretation Introduction

Interpretation:

The other mixture of alkyl halide and sulfide that yield from the same sulfonium salt that ismentioned exampleand the selection of the combination of mixture that forms faster than the other one is to be determined.

Concept Introduction:

Sulfur is stronger nucleophile than oxygen hence it reacts with alkyl halides faster than that of ethers. The reaction of alkyl halide and sulfur follows SN2 (nucleophilic substitution) reaction and results in the formation of sulfonium salt.

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You are asked to use curved arrows to generate the significant resonance structures for the following series of compounds and to label the most significant contributor. Identify the errors that would occur if you do not expand the Lewis structures or double-check the mechanisms. Also provide the correct answers.
how to get limiting reactant and % yield based off this data Compound Mass 6) Volume(mL Ben zaphone-5008 ne Acetic Acid 1. Sam L 2-propanot 8.00 Benzopin- a col 030445 Benzopin a Colone 0.06743 Results Compound Melting Point (°c) Benzopin acol 172°c - 175.8 °c Benzoping to lone 1797-180.9
Assign ALL signals for the proton and carbon NMR spectra on the following pages.

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