[References] his reaction is an example of conjugate addition of a nucleophile to an a.B-unsaturated carbonyl. NH2 0 NH3 CH3CH2CH2CH=CHËSCOA CH3CH2CH,CHCH2CSCOA Draw the two resonance structures of the enolate anion intermediate for this reaction.

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Draw the two resonance structures of the enolate anion intermediate for this reaction. 

[References]
This reaction is an example of conjugate addition of a nucleophile to an a ß-unsaturated carbonyl.
NH2
NH3
CH3CH2CH2CH=CHÖSCOA
CH3CH2CH2CHCH2CSCOA
Draw the two resonance structures of the enolate anion intermediate for this reaction.
• Draw an R1 group in place of CoA. The R group tool is located in the charges and lone pairs drop-down menu.
• Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.
• Separate resonance structures using the symbol from the drop-down menu.
P.
opy
aste
Transcribed Image Text:[References] This reaction is an example of conjugate addition of a nucleophile to an a ß-unsaturated carbonyl. NH2 NH3 CH3CH2CH2CH=CHÖSCOA CH3CH2CH2CHCH2CSCOA Draw the two resonance structures of the enolate anion intermediate for this reaction. • Draw an R1 group in place of CoA. The R group tool is located in the charges and lone pairs drop-down menu. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. • Separate resonance structures using the symbol from the drop-down menu. P. opy aste
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