(b) Draw the structure of the product formed by treating the Wittig reagent from part (a) with cyclopentanone. On [F ? ChemDoodle (c) Draw the structures of the products formed by hydrolyzing the enol ether from part (b) with HI. - [F √n Wittig reactions with a-chloroethers can be used for the synthesis of aldehydes and ketones. 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. (a) Draw the structure of the Wittig reagent formed from the following chloroether. CH3 CICHOCH2CH=CH2 √n [F
(b) Draw the structure of the product formed by treating the Wittig reagent from part (a) with cyclopentanone. On [F ? ChemDoodle (c) Draw the structures of the products formed by hydrolyzing the enol ether from part (b) with HI. - [F √n Wittig reactions with a-chloroethers can be used for the synthesis of aldehydes and ketones. 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. (a) Draw the structure of the Wittig reagent formed from the following chloroether. CH3 CICHOCH2CH=CH2 √n [F
(b) Draw the structure of the product formed by treating the Wittig reagent from part (a) with cyclopentanone. On [F ? ChemDoodle (c) Draw the structures of the products formed by hydrolyzing the enol ether from part (b) with HI. - [F √n Wittig reactions with a-chloroethers can be used for the synthesis of aldehydes and ketones. 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. (a) Draw the structure of the Wittig reagent formed from the following chloroether. CH3 CICHOCH2CH=CH2 √n [F
Wittig reactions with α-chloroethers can be used for the synthesis of aldehydes and ketones.
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.
(a)
Draw the structure of the Wittig reagent formed from the following chloroether.
(b)
Draw the structure of the product formed by treating the Wittig reagent from part (a) with cyclopentanone.
(c)
Draw the structures of the products formed by hydrolyzing the enol ether from part (b) with HI.
Transcribed Image Text:(b)
Draw the structure of the product formed by treating the Wittig reagent from part (a) with cyclopentanone.
On [F
?
ChemDoodle
(c) Draw the structures of the products formed by hydrolyzing the enol ether from part (b) with HI.
- [F
√n
Transcribed Image Text:Wittig reactions with a-chloroethers can be used for the synthesis of aldehydes and ketones.
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.
(a) Draw the structure of the Wittig reagent formed from the following chloroether.
CH3
CICHOCH2CH=CH2
√n [F
Definition Definition Organic compounds that have a carbonyl group, C=O, as their functional group. The carbonyl group in aldehydes is placed at the end of the molecular structure, which means the C=O is attached to one hydrogen atom and an alkyl group or a benzene ring. Just like all the other homologous series in organic chemistry, the naming of aldehydes uses the suffix “-al”. The general molecular formula is C n H 2n O.
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