Please select the correct name for the molecule at the top. Make sure the correct stereochemistry is indicated.(Z)-3,4,dimethylhept-3-ene(E)-3,4,dimethylhept-3-ene(Z)-4,5,dimethylhept-4-ene(E)-4,5,dimethylhept-4-ene The reaction below precedes via an E2 elimination versus an SN2 reaction. Circle all of the answers that correctly support this reaction outcome.NaOCH3+ NaCiCICH;OHThe nucleophilicity of the methoxide anion (CH30") is reduced in protic solventThe primary alkyl halide provides too much sterics for an effective SN2 reaction to occurSodium methoxide (NaOCH3) is a strong enough base to deprotonate the alkyl chlorideStable primary carbocations can formbeta-hydrogens on the carbon adjacent to the chloro group are available for deprotonation

In the case of the naming of alkene when two groups with major priority are present on the same side…

Please select the correct name for the molecule at the top. Make sure the correct stereochemistry is indicated. (Z)-3,4,dimethylhept-3-ene (E)-3,4,dimethylhept-3-ene (Z)-4,5,dimethylhept-4-ene (E)-4,5,dimethylhept-4-ene O O O

Please select the correct name for the molecule at the top. Make sure the correct stereochemistry is indicated. (Z)-3,4,dimethylhept-3-ene (E)-3,4,dimethylhept-3-ene (Z)-4,5,dimethylhept-4-ene (E)-4,5,dimethylhept-4-ene O O O

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter9: Addition Via Cyclic Intermediate

Section: Chapter Questions

Problem 3CTQ

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Question

Please select the correct name for the molecule at the top. Make sure the correct stereochemistry is indicated.
(Z)-3,4,dimethylhept-3-ene
(E)-3,4,dimethylhept-3-ene
(Z)-4,5,dimethylhept-4-ene
(E)-4,5,dimethylhept-4-ene

The reaction below precedes via an E2 elimination versus an SN2 reaction. Circle all of the answers that correctly support this reaction outcome.
NaOCH3
+ NaCi
CI
CH;OH
The nucleophilicity of the methoxide anion (CH30") is reduced in protic solvent
The primary alkyl halide provides too much sterics for an effective SN2 reaction to occur
Sodium methoxide (NaOCH3) is a strong enough base to deprotonate the alkyl chloride
Stable primary carbocations can form
beta-hydrogens on the carbon adjacent to the chloro group are available for deprotonation

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