Answer: NA and F would form an ionic bond
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Answer:
2-methylene propylbenzene
Explanation:
The Wittig Reaction is a reaction that converts aldehydes and ketones into alkenes through reaction with a phosphorus ylide.
The ketone in this case is 1-phenylpropan-1-one. The provided phosphonium ylide is shown in the image attached. The reaction involves;
i) alkylation
ii) addition
The product of the major organic product of the reaction is 2-methylene propylbenzene.
Answer:
Most substituted alkene is produced as a major product
Explanation:
- Dehydration of 3-methyl-2-butanol proceeds through E1 mechanism to form alkenes.
- Most substituted alkene is produced as major product because of presence of highest number of hyperconjugative hydrogen atoms corresponding to the produced double bond (Saytzeff product).
- Here, a H-shift also occurs in one of the intermediate step during dehydration to produce more stable tertiary carbocation.
- Reaction mechanism has been shown below.
Answer:
Please find the explanation to this question below.
Explanation: