Obrandi.jamyaLiked your me: HAPPY BIRTHDAY!!nowThis proposed alpha-alkylation reaction would not work. Identify what is wrong with it.1. LiNi-Pr₂/THF2. CH3CH2BrTap here or pull up for additional resourcesACH3BThis reaction would require a different solvent.The wrong base was used.There is a problem with the order of addition.SubmitDThe nucleophile isn't appropriate for this electrophile. Question 30 of 85This proposed alpha-alkylation reaction would not work. Identify what is wrong with it.1. NaH/THF2. CH3CH₂BrTap here or pull up for additional resourcesCACH3This reaction would require a different solvent.SubmitBThe wrong base was used.CThere is a problem with the order of addition.D The nucleophile isn't appropriate for this electrophile.

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This proposed alpha-alkylation reaction would not work. Identify what is wrong with it. 1. LiN¹-Pr₂/THF 2. CH3CH₂Br A CH3 B This reaction would require a different solvent. The wrong base was used. There is a problem with the order of addition. D The nucleophile isn't appropriate for this electrophile.

This proposed alpha-alkylation reaction would not work. Identify what is wrong with it. 1. LiN¹-Pr₂/THF 2. CH3CH₂Br A CH3 B This reaction would require a different solvent. The wrong base was used. There is a problem with the order of addition. D The nucleophile isn't appropriate for this electrophile.

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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13 saved out of on 14 r saved out of Given the following substitution reaction, what would the effect be of changing the solvent from DMF to CH₂OH? (see NOTE) *NOTE: DMF - NaOCH3 H-C-N(CH3)2 OCH 3 Select one: OA. There would be no effect on the reaction rate. OB. The rate of the reaction would increase. OC. The rate of the reaction would decrease. Clear my choice + Na Br In substitution reactions, (CH3)3C-I reacts at the same rate with Brand CI even though Br is a more reactive nucleophile than Cl. Why? max