don 13.(1) Draw the (E)- and (Z)- isomers of 1,3-dichloro-2-methylbut-2-ene.Using curved arrows, draw (a) an SN2 mechanism and (b) and SN1 mechanism for thesubstitution reaction shown below.Br) Draw the organic product(s) formed in the following reactions:1)0,by2) Zn. H,0MShow a sequence of reactions that could be used to synthesize the following compound.You must start from 3-pentanol. No mechanisms needed (HINT: You wil need to bring togethermore than one of the reactions you have seen in Modules 3 and 4]

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(1) Draw the (E)- and (Z)- isomers of 1,3-dichloro-2-methylbut-2-ene. Using curved arrows, draw (a) an SN2 mechanism and (b) and SN1 mechanism for the substitution reaction shown below. Br G) Draw the organic product(s) formed in the following reactions: Br/ HyO 1)0 2) Zn. H,0 by M Show a sequence of reactions that could be used to synthesize the following compound. You must start forom 3-pentanol. No mechanisms needed. (HINT: You will need to bring together more than one of the reactions you have seen in Módules 3 and 4)

(1) Draw the (E)- and (Z)- isomers of 1,3-dichloro-2-methylbut-2-ene. Using curved arrows, draw (a) an SN2 mechanism and (b) and SN1 mechanism for the substitution reaction shown below. Br G) Draw the organic product(s) formed in the following reactions: Br/ HyO 1)0 2) Zn. H,0 by M Show a sequence of reactions that could be used to synthesize the following compound. You must start forom 3-pentanol. No mechanisms needed. (HINT: You will need to bring together more than one of the reactions you have seen in Módules 3 and 4)

Organic Chemistry: A Guided Inquiry

2nd Edition

ISBN:9780618974122

Author:Andrei Straumanis

Publisher:Andrei Straumanis

Chapter24: Carboxylic Acids & Derivatives

Section: Chapter Questions

Problem 12CTQ

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