Answer the following questions related to organic reactions a) Identify the nucleophile, electrophile and leaving group when bromocyclohexane reacts with sodium cyanide. b) Draw the expected product(s) resulting from the following SN2 reaction: 3-iodoheptane and KOH c) Draw the expected product(s) resulting from the following SN1 reaction: 1-chloro-1-phenylethane and (CH3)2NH

Answer the following questions related to organic reactions a) Identify the nucleophile, electrophile and leaving group when bromocyclohexane reacts with sodium cyanide. b) Draw the expected product(s) resulting from the following SN2 reaction: 3-iodoheptane and KOH c) Draw the expected product(s) resulting from the following SN1 reaction: 1-chloro-1-phenylethane and (CH3)2NH

Organic Chemistry

8th Edition

ISBN:9781305580350

Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Publisher:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote

Chapter6: Reactions Of Alkenes

Section: Chapter Questions

Problem 6.31P: When 2-pentene is treated with Cl2 in methanol, three products are formed. Account for the formation...

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The SN2 reaction is an example of a nucleophilic substitution reaction. Draw the structure of the two reactants and the mechanism of the reaction. The reaction is 1-bromo-3-ethylpentane reacts with cyclohexanol under basic conditions.
Draw the substitution product formed when cis-1-bromo-4-methylcyclohexane and hydroxide ion undergo an SN2 reaction.
Draw the organic product(s) formed upon the addition of HBr to (a) 2-methyl-2-pentene, (b) trans-2-hexene, and (c) 4-methylcyclohexene. How many regioisomers can be formed in each case?
name and draw the product/s formed from the reaction of 3-methylpent-2-ene: 1. with HBr 2. with Cl2 3. H2O in the presence of H2SO4 4. ethanol in the presence of H2SO4 5. Br2, H2O 6. [1] 9-BBN; [2] H2O2, OH-
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Fill in the blank: The acid catalyzed hydration of alkenes (addition of H2O/H2SO4) is: A) a polar mechanism with carbocation intermediate B) a radical mechanism with carbon radical intermediate C) a concerted reaction
Dehydration of 1,2,2-trimethylcyclohexanol with H2SO4 affords 1-tertbutylcyclopentene as a minor product. (a) Draw a stepwise mechanism that shows how this alkene is formed. (b) Draw other alkenes formed in this dehydration. At least one must contain a five-membered ring.
Answer the following questions involving organic synthesis: a.) Propose a forward synthesis of an alkyne from an alkene starting material. b.) Develop a forward synthesis of an epoxide from 1-chloropropane. c.) Write a reasonable forward synthesis for the conversion of 2-bromopentane to ethyl methyl ether. d.) Write any reaction with an alkene that occurs via a syn addition and draw its transition state. e.) Write any reaction with an alkene that occurs via an anti addition and draw its transition state. f.) Define Markovnikov’s rule and write out two reactions: one that is a Markovnikov addition and another that is an anti-Markovnikov pathway.
Illustrate the structure of the compounds using the following:A. major product between 1,4-dimethylcyclohex-1-ene and BH3, H202, OH-B. major product Of 4-methylpent-2-ene reacted with mCPBA, H20, H+C. major product between 1-methylcyclobut-1-ene and Br2 in dark conditionsD. alkene that formed propanone and carbon dioxide upon reaction with O3, Zn, H2O, H+
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Draw all possible products formed when 2-methylbut-2-ene undergoes addition with HCl. Label them as being either the major or the minor product.