EP ORGANIC CHEMISTRY -MOD.MASTERING 18W
EP ORGANIC CHEMISTRY -MOD.MASTERING 18W
9th Edition
ISBN: 9780136781776
Author: Wade
Publisher: PEARSON CO
bartleby

Concept explainers

Question
Book Icon
Chapter 11.3, Problem 11.5P

(a)

Interpretation Introduction

To determine: The product of the given starting material with excess chromic acid.

Interpretation: The product of the given starting material with excess chromic acid is to be predicted.

Concept introduction: Chromic acid (H2CrO4) obtained from Na2Cr2O7/H2SO4, is used for the conversion of primary alcohol into carboxylic acid, and secondary alcohol into ketone.

(b)

Interpretation Introduction

To determine: The product of the given starting material with excess PCC.

Interpretation: The product of the given starting material with excess PCC is to be predicted.

Concept introduction: PCC is used for the conversion of primary alcohol into aldehyde, and secondary alcohol into ketone.

(c)

Interpretation Introduction

To determine: The product of the given starting material with excess NaOCl/CH3COOH.

Interpretation: The product of the given starting material with excess NaOCl/CH3COOH is to be predicted.

Concept introduction: Sodium hypochlorite and acetic acid (NaOCl/CH3COOH) is used for the conversion of primary alcohol into carboxylic acid, and secondary alcohol into ketone.

(d)

Interpretation Introduction

To determine: The product of the given starting material with excess DMSO,COCl2.

Interpretation: The product of the given starting material with excess DMSO,COCl2 is to be predicted.

Concept introduction: DMSO,COCl2 is used for the conversion of primary alcohol into aldehyde, and secondary alcohol into ketone.

(e)

Interpretation Introduction

To determine: The product of the given starting material with excess DMP.

Interpretation: The product of the given starting material with excess DMP is to be predicted.

Concept introduction: DMP is used for the conversion of primary alcohol into aldehyde, and secondary alcohol into ketone.

Blurred answer
Students have asked these similar questions
What compounds are formed from the reaction of benzoyl chloride with the following reagents? a. sodium acetate    b. water                     c. excess dimethylamine d. aqueous HCl        e. aqueous NaOH      f. cyclohexanol g. excess benzylamine h. 4-chlorophenol i. isopropyl alcohol j. excess aniline             k. potassium formate
Which of the following reagents will not undergo a substitution reaction with the benzenediazonium chloride salt.    A.  H3PO2 , H2O  B.  KI  C.  H3PO3, H2O  D.  Cu2O, Cu+2, H2O  E.  CuCN
Phosgene (COCl2) was used as a poison gas in World War I. What product would be formed from the reaction of phosgene with each of the following reagents? a. one equivalent of methanol b. excess methanol c. excess propylamine d. excess water

Chapter 11 Solutions

EP ORGANIC CHEMISTRY -MOD.MASTERING 18W

Ch. 11.6 - Predict the products of the following reactions....Ch. 11.7A - Propose a mechanism for the reaction of a....Ch. 11.7B - Prob. 11.13PCh. 11.7B - Show how you would use a simple chemical test to...Ch. 11.7C - Neopentyl alcohol, (CH3)3CCH2OH, reacts with...Ch. 11.7C - Prob. 11.16PCh. 11.7C - When cis-2-methylcyclohexanol reacts with the...Ch. 11.8 - Prob. 11.18PCh. 11.9 - Prob. 11.19PCh. 11.9 - Prob. 11.20PCh. 11.9 - Prob. 11.21PCh. 11.10A - Prob. 11.22PCh. 11.10A - Some alcohols undergo rearrangement or other...Ch. 11.10B - Prob. 11.24PCh. 11.10B - Explain why the acid-catalyzed condensation is a...Ch. 11.10B - Prob. 11.26PCh. 11.10B - When the following substituted cycloheptanol...Ch. 11.11A - Prob. 11.28PCh. 11.11A - Prob. 11.29PCh. 11.11B - Predict the products formed by periodic acid...Ch. 11.12 - Prob. 11.31PCh. 11.13A - Prob. 11.32PCh. 11.14 - Prob. 11.33PCh. 11.14 - a. Show how ethanol and cyclohexanol may be used...Ch. 11.14 - Prob. 11.35PCh. 11.14 - Phenols (pKa 10) are more acidic than other...Ch. 11.14 - To practice working through the early parts of a...Ch. 11.14 - Prob. 11.38PCh. 11 - Predict the major products of the following...Ch. 11 - Show how you would convert 2-methylcyclopentanol...Ch. 11 - In each case, show how you would synthesize the...Ch. 11 - Prob. 11.42SPCh. 11 - Prob. 11.43SPCh. 11 - Prob. 11.44SPCh. 11 - Both cis- and trans-2-methylcyclohexanol undergo...Ch. 11 - Prob. 11.46SPCh. 11 - Prob. 11.47SPCh. 11 - Show how you would make each compound, beginning...Ch. 11 - Predict the major products (including...Ch. 11 - Show how you would use simple chemical tests to...Ch. 11 - The compound shown below has three different types...Ch. 11 - Prob. 11.52SPCh. 11 - Prob. 11.53SPCh. 11 - Prob. 11.54SPCh. 11 - Prob. 11.55SPCh. 11 - Show how you would synthesize the following...Ch. 11 - Show how you would synthesize the following...Ch. 11 - The following pseudo-syntheses (guaranteed not to...Ch. 11 - Two unknowns, X and Y, both having the molecular...Ch. 11 - The Williamson ether synthesis involves the...Ch. 11 - Prob. 11.61SPCh. 11 - Prob. 11.62SPCh. 11 - Alcohols combine with ketones and aldehydes to...Ch. 11 - Prob. 11.64SPCh. 11 - Prob. 11.65SPCh. 11 - Prob. 11.66SP
Knowledge Booster
Background pattern image
Chemistry
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
  • Text book image
    Organic Chemistry
    Chemistry
    ISBN:9781305580350
    Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
    Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9781305580350
Author:William H. Brown, Brent L. Iverson, Eric Anslyn, Christopher S. Foote
Publisher:Cengage Learning