Chem Assignment 6

Chem Assignment 6 - Question 6.13.3 Choose the reagent below that would be the best to convert propyl bromide into CH3CH2OCH2CH2CH3 CH3CH2OH

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Question 6.13.3 Choose the reagent below that would be the best to convert propyl bromide into CH 3 CH 2 OCH 2 CH 2 CH 3 CH 3 CH 2 OH CH 3 CH 2 Cl CH 3 CH 2 CH 2 ONa CH 3 CH 2 CH 2 OH KOCH 2 CH 3 Question 6.13.5 Choose the reagent below that would be the best to convert propyl bromide into CH 3 CH 2 CH 2 CN KCN CH 3 CN NH 3 HCN NaN 3 Question 6.14.1 Answer the following questions: Select the alkyl halide that you would expect to react more rapidly in an S N 2 reaction. Select the all explanations that apply to your choice in part (a). The carbon attached to the leaving group is the less sterically hindered The compound is a primary alkyl halide The compound would give the most stable carbocation The compound has a better leaving group. The compound is a secondary alkyl halide The compound is a tertiary alkyl halide Question 6.15.2 Select the SN2 reaction you would expect to take place more rapidly in a protic solvent.
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Question 6.15.4 Select the S N 2 reaction you would expect to take place more rapidly in a protic solvent. Question 6.18.1
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This note was uploaded on 09/13/2011 for the course CHEM 233 taught by Professor Daub during the Spring '09 term at Waterloo.

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Chem Assignment 6 - Question 6.13.3 Choose the reagent below that would be the best to convert propyl bromide into CH3CH2OCH2CH2CH3 CH3CH2OH

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