Question

Wittig reactions with a-chloroethers can be used for the synthesis of aldehydes and ketones. An enol ether is formed by treat

Wittig reactions with α-chloroethers can be used for the synthesis of aldehydes and ketones.

An enol ether is formed by treating cyclohexanone with the Wittig reagent derived from this chloroether. Draw the structures of the products formed when this enol ether is hydrolyzed with HI.

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  • Ignore alkene stereochemistry.
  • When drawing products of Wittig reactions, draw only the alkene formed, do not include triphenylphosphine oxide.
  • Draw Wittig reagents in ylide form.
  • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.
  • Separate structures with + signs from the drop-down menu.
Wittig reactions with a-chloroethers can be used for the synthesis of aldehydes and ketones. An enol ether is formed by treating cyclohexanone with the Wittig reagent derived from this chloroether. Draw the structures of the products formed when this enol ether is hydrolyzed with HI CICH2OCH2CH-CH2 Ignore alkene stereochemistry. When drawing products of Wittig reactions, draw only the alkene formed, do not include triphenylphosphine oxide. Draw Wittig reagents in ylide form. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate structures with+signs from the drop-down menu.
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qiven that, triphenyl phexphine to orm an interme diate neagent phos phonium A!ドyl chloride reac t lth triphenyl Salt os phoform enol E no alkyl iodide as Product The Enol tunde goes heto- enol tau to merism fom alde hyde Enol ene Thus, the pnoductr

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