20:25 : E) Grignard 16. Acid chlorides can be prepared from carboxylic acids by treatment with A) KCI B) (COCI)2 C) SOCI₂ D) both (COCI)2 and SOCI₂ E) both SOCI₂ and KCI 17. Provide the major organic product of the reaction shown. Find your most reactive electrons. Where will they go? Check to see if the intermediate has a good leaving group. If so, check to see if you have enough of the nucleophile to repeat nucleophilic attack. 1. Me-MgBr (xs) 2. H₂O+ Send a chat O

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20:25
:
E) Grignard
16. Acid chlorides can be prepared from carboxylic acids by treatment with
A) KCI
B) (COCI)2
C) SOCI₂
D) both (COCI)2 and SOCI₂
E) both SOCI₂ and KCI
17. Provide the major organic product of the reaction shown.
Find your most reactive electrons. Where will they go?
Check to see if the intermediate has a good leaving group.
If so, check to see if you have enough of the nucleophile to repeat nucleophilic
attack.
1. Me-MgBr (xs)
2. H₂O+
Send a chat
O
Transcribed Image Text:20:25 : E) Grignard 16. Acid chlorides can be prepared from carboxylic acids by treatment with A) KCI B) (COCI)2 C) SOCI₂ D) both (COCI)2 and SOCI₂ E) both SOCI₂ and KCI 17. Provide the major organic product of the reaction shown. Find your most reactive electrons. Where will they go? Check to see if the intermediate has a good leaving group. If so, check to see if you have enough of the nucleophile to repeat nucleophilic attack. 1. Me-MgBr (xs) 2. H₂O+ Send a chat O
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