(b)Problem 10-33Draw resonance structures for the following species:+(a)CH3CH=CHCH=CHCH=CHCH2+(c)CH3C=N-ÖCS Scanned with CamScanner14

Step 1:The resonance structures are drawn when a single Lewis structure fails to explain all the…

Answered: (b) Problem 10-33 Draw resonance…

Organic Chemistry

9th Edition

ISBN:9781305080485

Author:John E. McMurry

Publisher:John E. McMurry

Chapter7: Alkenes: Structure And Reactivity

Section7.SE: Something Extra

Problem 29MP: When methyl vinyl ether reacts with a strong acid, the proton adds to C2 exclusively, instead of C1...

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(CH3)3C- (CHa)3C Br Br cis-1-bromo-4-tert-butylcyclohexane trans-1-bromo-4-tert-butylcyclohexane a. The cis and trans isomers of 1-bromo-4-tert-butylcyclohexane react at different rates with KOC(CH)3 to afford the same mixture of enantiomers A and B. Draw the structures of A and B. b. Which isomer reacts faster with KOC(CHa)g? Offer an explanation for this difference in reactivity. c. Reaction of cis-1-bromo-4-tert-butylcyclohexane with NAOCH3 affords C as the major product, whereas reaction of trans-1-bromo-4-tert-butylcyclohexane affords D as the major product. Draw the structures for C and D. d. The cis and trans isomers react at different rates with NaOCH3. Which isomer reacts faster? Offer an explanation for the difference in reactivity. e. Why are different products formed from these alkyl halides when two different alkoxides are used as reagents?
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(b) Problem 10-33 Draw resonance structures for the following species: + (a) CH3CH=CHCH=CHCH=CHCH2 + (c) CH3C=N-Ö CS Scanned with CamScanner 1 4