Organic Chemistry
Organic Chemistry
12th Edition
ISBN: 9781118875766
Author: T. W. Graham Solomons, Craig B. Fryhle, Scott A. Snyder
Publisher: WILEY
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Chapter 12, Problem 28P

For each of the following alcohols, write a retrosunthetic analysis and synthesis that involves an appropriate organometallic reagent (either a Grignard or alkyllithium reagent).

(a)

Chapter 12, Problem 28P, For each of the following alcohols, write a retrosunthetic analysis and synthesis that involves an , example  1

(b)

Chapter 12, Problem 28P, For each of the following alcohols, write a retrosunthetic analysis and synthesis that involves an , example  2

(c)

Chapter 12, Problem 28P, For each of the following alcohols, write a retrosunthetic analysis and synthesis that involves an , example  3

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Q3: Curved Arrows, Lewis Acids & Bases, Nucleophiles and Electrophiles Considering the following reactions: a) Predict the products to complete the reactions. b) Use curved electron-pushing arrows to show the mechanism for the reaction in the forward direction. Redraw some of the compounds to explicitly illustrate all bonds that are broken and all bonds that are formed. c) Label Lewis acids and bases, nucleophiles and electrophiles in the reactions. A. S + AICI 3 B. + H₂O
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Naming the Alkanes a) Write the IUPAC nomenclature of the compound below b) Draw 4-isopropyl-2,4,5-trimethylheptane, identify the primary, secondary, tertiary, and quaternary carbons. c) Rank pentane, neopentane and isopentane for boiling point. pentane: H3C-CH2-CH2-CH2-CH3 neopentane: CH3 H3C-Ċ-CH3 I CH3 isopentane: CH3 H3C-CH2-CH-CH3

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Organic Chemistry

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