Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second)
Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second)
2nd Edition
ISBN: 9780393655551
Author: KARTY, Joel
Publisher: W. W. Norton & Company
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Chapter 14, Problem 14.58P
Interpretation Introduction

Interpretation:

The complete, detailed mechanism for the given reaction is to be drawn, and the major product is to be predicted.

Concept introduction:

The conjugate bases of weak acids like alcohol can behave as both a strong base and a good nucleophile. In poar aprotic solvents, a secondary alkyl halide with good leaving group can undergo both nucleophilic substitution (SN2) and elimination (E2). The temperature at which the reaction is carried out determines which mechanism is favored and, therefore, the major product that is formed. A low temperature favors substitution while high temperatures favor elimination.

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PLEASE READ!!! I DONT WANT EXAMPLES, I DONT WANT WORDS OR PARAGRAPHS FOR THE MECHANISM!!! THANKS First image: QUESTION 6. I have to show, with ARROWS and STRUCTURES, the mechanism of the reaction at the bottom. Also I have to show by mecanism why the reaction wouldn't work if the alcohol was primary. I also tried to draw the mechanism, tell me what to change. Please note that its an AMIDE thats formed not an AMINE the nitrogen has ONE hydrogen and one Phenyl-C-Phenyl. I already asked for this mechanism and got as a final product ...-NH2 not whats shown on the picture, thank you Ths second part. QUESTION 3. I just need a way to synthesize the lactone A, I already started please continue from where I left it  Second image: I simply need the products, substrates or reagents, thank you
Indicate how to prepare a 10% sodium hydroxide (NaOH) solution to a slightly alkaline pH.

Chapter 14 Solutions

Organic Chemistry: Principles And Mechanisms: Study Guide/solutions Manual (second)

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