The following reaction does not produce the desired product but does produce a product that is a constitutional isomer of the desired product. Draw the product that is obtained and propose a mechanism for its formation: OH OH 1) NaNH, 2) MeI 09.70a Modify the given structure to draw the product of this reaction. Do not use abbreviations when drawing the product. OH CH Edit Drawing

Q: select the major 1. NaOCH2CH3 CH3CH2OH CH3CH30 OCH2CH3 2. H3o+ OCH2CHS OCH2CH

A: The given reaction is an example of an intramolecular Claisen condensation reaction.

Q: 2 Draw the major product of this reaction. Ignore inorganic byproducts. 1. (CH3CH2)2CuLi 2. H3O+…

A: Product of the reaction

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Q: NaOH 12 excess

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A: Step 1:Here is the step  1 mechanism and the intermediate product  Computer typed version:

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Q: Alcohols OH OH

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Q: Br Br 1) 3 NaNH, 2) Butanone 3) H3O+

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Q: (h) CH, CO CH,CO,H, 50 Draw the major product(s) of the reaction. H₂C CH3 Edit Drawing Draw the…

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Q: охсхо 11 III F NV + : -CH₂ (X) -CH₂ н, с CH₂ CH₂ I P S F CI Br 0 Т с N

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Q: HBr Br HO 65°C

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A: The mechanism has been drawn below

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A:

Reactions at the Alpha Carbon Atom

The position next to the ketone or aldehyde functional group is termed as alpha position and the reaction which occurs at alpha position is called alpha substitution reaction. In an alpha substitution reaction, the alpha proton atom is substituted by an electrophile by the formation of an enol intermediate or enolate ion intermediate. Most of the carbonyl compounds go through an alpha substitution reaction.