ORGANIC CHEM. PRIN AND MECHANISM LL+ AC
ORGANIC CHEM. PRIN AND MECHANISM LL+ AC
2017th Edition
ISBN: 9780393630787
Author: KARTY
Publisher: W.W.NORTON+CO.
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Chapter 12, Problem 12.1YT
Interpretation Introduction

Interpretation:

To find out how many single bonds each C atom has and how many bonds a double bond represents.

Concept introduction:

If the electrophilic atom on the electrophile has a lone pair of electrons, then addition can take place in a way that avoids losing an octet. E represents a generic electrophile that possesses a lone pair of electrons. Two new E-C σ bonds are formed simultaneously to produce a three-membered ring. One of those is formed by the electrons from the initial carbon-carbon π bond, and the other is formed by the lone pair of electrons from the electrophile.

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Using Zaitsev's rule, choose the most stable alkene among the following. Draw out the structures of each of the options then select the correct answer. Recall that Zaitsev's Rule is about alkene stability. The trend for this is similar to the trend for carbocation stability. Either more or fewer groups on the alkene (and the carbocation) make it more stable. This question is wanting you to remember if it's more or fewer. A) 1,2-dimethylcyclohexene B) 1,6-dimethylcyclohexene C) cis-3,4-dimethylcyclohexene D) They are all of equal stability according to Zaitsev's rule. Provide the major dehydration product of the following reaction. Recall which of the four substitution and elimination reactions a dehydration is. Before you do your S# or EF mechanism, remember what heteroatoms do in the presence of an acid (aka-the-OH is a bad leaving group, but protonating it might turn it into a good one). Don't forget to apply the concept from the previous question. OH Ht A

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ORGANIC CHEM. PRIN AND MECHANISM LL+ AC

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