ORGANIC CHEMISTRY MASTERINGCHEM ACCESS
ORGANIC CHEMISTRY MASTERINGCHEM ACCESS
9th Edition
ISBN: 9780137249442
Author: Wade
Publisher: INTER PEAR
bartleby

Concept explainers

Question
Book Icon
Chapter 8, Problem 8.65SP

(a)

Interpretation Introduction

To determine: The conversion of fumaric acid to (±)tartaricacid.

Interpretation: The given question stated that two butenedioic acids are called fumaric acids (trans) and maleic acid (cis) and 2,3Dihydroxybutanedioicacid is called tartaric acid. The given conversion is to be predicted.

Concept introduction: Osmium tetroxide also called osmic acid reacts with alkenes to form cyclic osmate ester. Hydrogen peroxide is used as an oxidizing agent to hydrolyze the osmate ester. The attack of oxygen from osmic acid to the double bond of alkene is from the same side. Thus they have syn stereochemistry.

(b)

Interpretation Introduction

To determine: The conversion of fumaric acid to meso-tartaric acid.

Interpretation: The given question stated that two butenedioic acids are called fumaric acids (trans) and maleic acid (cis) and 2,3Dihydroxybutanedioicacid is called tartaric acid. The given conversion is to be predicted.

Concept introduction: Epoxidation of alkene is an oxidation process. Epoxides are also called an oxirane and they are intermediates that are used to convert alkenes into other functional group. Peroxyacid is used to convert alkene into an epoxide.

The steps followed by the given reaction are stated as:

  • First step is the formation of epoxide.
  • Second step is the attack of water to opens the ring.
  • The third step is deprotonation that gives diol product.

(c)

Interpretation Introduction

To determine: The conversion of maleic acid to (±)tartaricacid.

Interpretation: The given question stated that two butenedioic acids are called fumaric acids (trans) and maleic acid (cis) and 2,3Dihydroxybutanedioicacid is called tartaric acid. The given conversion is to be predicted.

Concept introduction: Epoxidation of alkene is an oxidation process. Epoxides are also called an oxirane and they are intermediates that are used to convert alkenes into other functional group. Peroxyacid is used to convert alkene into an epoxide.

The steps followed by the given reaction are stated as:

  • First step is the formation of epoxide.
  • Second step is the attack of water to opens the ring.
  • The third step is deprotonation that gives diol product.

(d)

Interpretation Introduction

To determine: The conversion of maleic acid to meso-tartaric acid.

Interpretation: The given question stated that two butenedioic acids are called fumaric acids (trans) and maleic acid (cis) and 2,3Dihydroxybutanedioicacid is called tartaric acid. The given conversion is to be predicted.

Concept introduction: Osmium tetroxide also called osmic acid reacts with alkenes to form cyclic osmate ester. Hydrogen peroxide is used as an oxidizing agent to hydrolyze the osmate ester. The attack of oxygen from osmic acid to the double bond of alkene is from the same side. Thus, they have syn stereochemistry.

Blurred answer
Students have asked these similar questions
First image: I have to show the mecanism (with arows and structures) of the reaction at the bottom. Also I have to show by mecanism why the reaction wouldn't work if the alcohol was primary Second image: I have to show the mecanism (with arrows and structures) for the reaction on the left, where the alcohol A is added fast in one portion its not an exam
what is the skeletal structure of a tertiary alkyl fluoride with six carbon atoms and no rings.
One step of glycolysis is a retro-aldol reaction (aldolase) to produce ATP.Below is the aldol reaction of the equilibrium. Show the mechanism for the base catalyzed reaction. *see image

Chapter 8 Solutions

ORGANIC CHEMISTRY MASTERINGCHEM ACCESS

Ch. 8.7A - Prob. 8.11PCh. 8.7C - Prob. 8.12PCh. 8.7C - Prob. 8.13PCh. 8.7C - a. When (Z)-3-methylhex-3-ene undergoes...Ch. 8.7C - Prob. 8.15PCh. 8.7C - Prob. 8.16PCh. 8.8B - Prob. 8.17PCh. 8.8B - Prob. 8.18PCh. 8.9 - Prob. 8.19PCh. 8.9 - Prob. 8.20PCh. 8.9 - Prob. 8.21PCh. 8.9 - Prob. 8.22PCh. 8.10 - Prob. 8.23PCh. 8.10 - Prob. 8.24PCh. 8.10 - Prob. 8.25PCh. 8.11A - Prob. 8.26PCh. 8.11B - Prob. 8.27PCh. 8.11B - Prob. 8.28PCh. 8.12 - Prob. 8.29PCh. 8.13 - a. Propose a mechanism for the conversion of...Ch. 8.13 - Magnesium monoperoxyphthalate (MMPP) epoxidizes...Ch. 8.13 - Predict the major products of the following...Ch. 8.13 - When 1,2-epoxycyclohexane (cyclohexene oxide) is...Ch. 8.14C - Predict the major products of the following...Ch. 8.14C - Prob. 8.35PCh. 8.15B - Prob. 8.36PCh. 8.15C - Predict the major products of the following...Ch. 8.16A - Prob. 8.38PCh. 8.16A - Prob. 8.39PCh. 8.16B - Prob. 8.40PCh. 8.16B - Prob. 8.41PCh. 8.16C - Prob. 8.42PCh. 8.17B - Prob. 8.43PCh. 8.17B - Prob. 8.44PCh. 8.17B - Show how you would synthesize each compound,...Ch. 8 - Prob. 8.46SPCh. 8 - Prob. 8.47SPCh. 8 - Give the products expected when the following...Ch. 8 - Show how you would make the following compounds...Ch. 8 - Using 1,2-dimethylcyclohexene as your starting...Ch. 8 - Show how you would synthesize each compound using...Ch. 8 - Prob. 8.52SPCh. 8 - Show how you might use olefin metathesis to...Ch. 8 - Prob. 8.54SPCh. 8 - Prob. 8.55SPCh. 8 - Propose mechanisms consistent with the following...Ch. 8 - Prob. 8.57SPCh. 8 - Prob. 8.58SPCh. 8 - Draw a reaction-energy diagram for the propagation...Ch. 8 - Prob. 8.60SPCh. 8 - Prob. 8.61SPCh. 8 - Prob. 8.62SPCh. 8 - Prob. 8.63SPCh. 8 - Prob. 8.64SPCh. 8 - Prob. 8.65SPCh. 8 - Prob. 8.66SPCh. 8 - Prob. 8.67SPCh. 8 - Prob. 8.68SPCh. 8 - Prob. 8.69SPCh. 8 - Prob. 8.70SPCh. 8 - Prob. 8.71SPCh. 8 - Prob. 8.72SPCh. 8 - Prob. 8.73SPCh. 8 - Prob. 8.74SPCh. 8 - Prob. 8.75SPCh. 8 - Prob. 8.76SPCh. 8 - Prob. 8.77SPCh. 8 - Prob. 8.78SPCh. 8 - Prob. 8.79SP
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.
Recommended textbooks for you
Text book image
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
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
Text book image
Chemistry for Today: General, Organic, and Bioche...
Chemistry
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Publisher:Cengage Learning