Homework Help is Here – Start Your Trial Now!
Science
Chemistry
22) what would be the alcohol product if MeMgBr/ether &H3O+ are added to 3-hexanone ?

22) what would be the alcohol product if MeMgBr/ether &H3O+ are added to 3-hexanone ?

Chemistry
Chemistry
10th Edition
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Chapter1: Chemical Foundations
Section: Chapter Questions
Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...
See similar textbooks
icon
Related questions
Question
22) what would be the alcohol product if MeMgBr/ether &H3O+ are added to 3-hexanone ? And 24-25
24) Which of the reducing agents produces 1,4-cyclohexadiene analogs from benzenes? (a) Sn/conc. HCI (b) Na/NH3 (c) H2/Raney Ni (d) NaBH4/E1OH (e) Zn-Hg/HCl(aq) 25) Circle alcohol(s), show the "strongest acid" due to “resonance-stabilized" conjugate base. 1-propen-1-ol cyclohexanol phenol 1-pentanol can be preferred to produce aldehyde by the oxidation of 2-methyl-1- 26) The reagent(s) pentanol? a) NaOCI/TEMPO (b) CrO3/H2SO4 (c) both PCC and Swern (d) KMNO4. 27) Which one of the following reactions is Fischer-Esterification? (b) 1-butanol/CH;CO,H (e) 1-butanal/EtCO,H (c) butan-2,3-diol/HNO3 а) 1-propanol/H;PО, d) 1-propanol/H,S04 -8) Circle the alcohol that is the most reactive towards Lucas reagent (HCl/ZnCl,)? HO, HO, HO P) Circle the "ether(s)" that need(s) excess HBr for the "ether-cleavage" process.
Transcribed Image Text:24) Which of the reducing agents produces 1,4-cyclohexadiene analogs from benzenes? (a) Sn/conc. HCI (b) Na/NH3 (c) H2/Raney Ni (d) NaBH4/E1OH (e) Zn-Hg/HCl(aq) 25) Circle alcohol(s), show the "strongest acid" due to “resonance-stabilized" conjugate base. 1-propen-1-ol cyclohexanol phenol 1-pentanol can be preferred to produce aldehyde by the oxidation of 2-methyl-1- 26) The reagent(s) pentanol? a) NaOCI/TEMPO (b) CrO3/H2SO4 (c) both PCC and Swern (d) KMNO4. 27) Which one of the following reactions is Fischer-Esterification? (b) 1-butanol/CH;CO,H (e) 1-butanal/EtCO,H (c) butan-2,3-diol/HNO3 а) 1-propanol/H;PО, d) 1-propanol/H,S04 -8) Circle the alcohol that is the most reactive towards Lucas reagent (HCl/ZnCl,)? HO, HO, HO P) Circle the "ether(s)" that need(s) excess HBr for the "ether-cleavage" process.
(b) 3-ethyl-3-hexanol (a) 3-methyl-2-hexanol hexanol. (c) 3-methyl-3-hexanol (d) 3-methyl-1- 23) Provide the structure of the major organic product in the reaction shown below 1. 2 CH3CH2CHMgBr H3 CHz CHz CT n OCH2CH3 2. H30* 3° alcohul 24) Which of the reducing agents produces 1,4-cyclohexadiene analogs from benzenes? (a) Sn/conc. HC1 (b) Na/NH3 (c) H2/Raney Ni (d) NABH4/EtOH (e) Zn-Hg/HCl(aq) 25) Circle alcohol(s), show the "strongest acid" due to "resonance-stabilized" conjugate base. 1-propen-1-ol cyclohexanol phenol 1-pentanol can be preferred to produce aldehyde by the oxidation of 2-meth= 5) The reagent(s) pentanol? NaOCI/TEMPO (b) CrO3/H2SO4 (c) both PCC and Swern (d) KMNO4. Which one of the following reactions is Fischer-Esterification?
Transcribed Image Text:(b) 3-ethyl-3-hexanol (a) 3-methyl-2-hexanol hexanol. (c) 3-methyl-3-hexanol (d) 3-methyl-1- 23) Provide the structure of the major organic product in the reaction shown below 1. 2 CH3CH2CHMgBr H3 CHz CHz CT n OCH2CH3 2. H30* 3° alcohul 24) Which of the reducing agents produces 1,4-cyclohexadiene analogs from benzenes? (a) Sn/conc. HC1 (b) Na/NH3 (c) H2/Raney Ni (d) NABH4/EtOH (e) Zn-Hg/HCl(aq) 25) Circle alcohol(s), show the "strongest acid" due to "resonance-stabilized" conjugate base. 1-propen-1-ol cyclohexanol phenol 1-pentanol can be preferred to produce aldehyde by the oxidation of 2-meth= 5) The reagent(s) pentanol? NaOCI/TEMPO (b) CrO3/H2SO4 (c) both PCC and Swern (d) KMNO4. Which one of the following reactions is Fischer-Esterification?
Expert Solution
steps

Step by step

Solved in 2 steps with 2 images

SEE SOLUTIONCheck out a sample Q&A here
Blurred answer
Knowledge Booster
Alkenes
Learn more about
Need a deep-dive on the concept behind this application? Look no further. Learn more about this topic, chemistry and related others by exploring similar questions and additional content below.
Similar questions
  • SEE MORE QUESTIONS
Recommended textbooks for you
Chemistry
Chemistry
Chemistry
ISBN:
9781305957404
Author:
Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:
Cengage Learning
Chemistry
Chemistry
Chemistry
ISBN:
9781259911156
Author:
Raymond Chang Dr., Jason Overby Professor
Publisher:
McGraw-Hill Education
Principles of Instrumental Analysis
Principles of Instrumental Analysis
Chemistry
ISBN:
9781305577213
Author:
Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:
Cengage Learning
Organic Chemistry
Organic Chemistry
Chemistry
ISBN:
9780078021558
Author:
Janice Gorzynski Smith Dr.
Publisher:
McGraw-Hill Education
Chemistry: Principles and Reactions
Chemistry: Principles and Reactions
Chemistry
ISBN:
9781305079373
Author:
William L. Masterton, Cecile N. Hurley
Publisher:
Cengage Learning
Elementary Principles of Chemical Processes, Bind…
Elementary Principles of Chemical Processes, Bind…
Chemistry
ISBN:
9781118431221
Author:
Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:
WILEY
SEE MORE TEXTBOOKS