Organic Chemistry Plus Masteringchemistry With Pearson Etext, Global Edition
Organic Chemistry Plus Masteringchemistry With Pearson Etext, Global Edition
9th Edition
ISBN: 9781292151229
Author: Wade, LeRoy G.
Publisher: PEARSON
bartleby

Concept explainers

Question
Book Icon
Chapter 25, Problem 25.15SP

(a)

Interpretation Introduction

To determine: The product obtained from the reaction of triolein with NaOH in water.

Interpretation: The product obtained from the reaction of triolein with NaOH in water is to be stated.

Concept introduction: The mixture of sodium hydroxide (Strong base) and water is used to convert ester into an ester salt of metallic sodium. The mechanism of the reaction comprises three steps. The first step is the addition of nucleophile. The second step is elimination of the leaving group. The third step is the deprotonation of carboxylic acid by methoxide ion.

(b)

Interpretation Introduction

To determine: The product obtained from the reaction of triolein with H2 and nickel catalyst.

Interpretation: The product obtained from the reaction of triolein with H2 and a nickel catalyst is to be stated.

Concept introduction: Hydrogen gas in the presence of metal catalyst is used to reduce unsaturated hydrocarbon to saturated hydrocarbon.

(c)

Interpretation Introduction

To determine: The product obtained from the reaction of triolein with Br2 in CCl4.

Interpretation: The product obtained from the reaction of triolein with Br2 in CCl4 is to be stated.

Concept introduction: The reaction of an alkene with Br2 in CCl4 results in the cleavage of double bond and thereby bromine atom attached to each carbon atom. The stereochemistry of the reaction is inversion of configuration.

(d)

Interpretation Introduction

To determine: The product obtained from the reaction of triolein with ozone and then dimethyl sulphide.

Interpretation: The product obtained from the reaction of triolein ozone and then dimethyl sulphide is to be stated.

Concept introduction: Ozonolysis is the oxidative cleavage of the double bond, where C=C bond breaks and hence formation of CO bond takes place. During oxidative cleavage, ketone or aldehyde formation takes place.

(e)

Interpretation Introduction

To determine: The product obtained from the reaction of triolein with warm KMnO4 in water.

Interpretation: The product obtained from the reaction of triolein with warm KMnO4 in water is to be stated.

Concept introduction: Potassium permanganate is a strong oxidising agent. In hot water it cleaves unsaturated hydrocarbon and convert it into acid.

(f)

Interpretation Introduction

To determine: The product obtained from the reaction of triolein with CH2I2/Zn(Cu).

Interpretation: The product obtained from the reaction of triolein with CH2I2/Zn(Cu) is to be stated.

Concept introduction: Simmons-smith reactions are those in which methylene iodide reacts with zinc-copper to gives a carbenoid which is known as Simmons-smith reagent. This carbenoid reacts with an alkene to give cyclopropane product.

Blurred answer
Students have asked these similar questions
He arranged the periodic table by their atomic masses and, predicted the existence of some elements missing in his periodic table correctly. Meyer Mendeleev Dobereiner Newlands 86. Fehling’s & Benedict’s reagents, used to determine the presence of reducing sugars contain which salt: NiSO4 SrSO4 MgSO4 CaSO4 CuSO4
What are the reagents used in Group 3 that will separate each of the following pairs? a. CoS, ZnS b. Fe3+, Al3+ NaOHc. Zn(NH3)2+, CrO42-d. Al3+, Zn2+
What reaction produces the following compound in good yield? a. Ethanoyl chloride + phenol in pyridineb. Acetic acid + phenol and sulfuric acidc. Acetic acid + benzened. Ethane + Sodium PhONa (Phenoxide) + Hot Sulfuric Acid
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