Organic Chemistry (9th Edition)
9th Edition
ISBN: 9780321971371
Author: Leroy G. Wade, Jan W. Simek
Publisher: PEARSON
expand_more
expand_more
format_list_bulleted
Question
Chapter 25.3A, Problem 25.2P
Interpretation Introduction
Interpretation: An equation for the complete hydrogenation of trilinolein in excess hydrogen and name of the product is to be stated. The approximate melting point of starting material and product is to be predicted.
Concept introduction: The process of conversion of double bond into single bond by the addition of
To determine: An equation for the complete hydrogenation of trilinolein in excess hydrogen, name of the product and approximate melting point of starting material and product.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solutionStudents have asked these similar questions
What reagents would you use to chemically extract benzoic acid and valeric acid? Or can it not be chemically extracted? The image shows the compound structure.
Kindly provide an explanation thank you
1. Give the oxidation products of the compound.
2. Possible routes of excretion for the compound.
Chapter 25 Solutions
Organic Chemistry (9th Edition)
Ch. 25.3 - Prob. 25.1PCh. 25.3A - Prob. 25.2PCh. 25.3B - Give an equaton for the complete transestenfcation...Ch. 25.4 - Prob. 25.4PCh. 25.4 - Several commercial laundry soaps contain...Ch. 25.4 - Prob. 25.6PCh. 25.4 - Prob. 25.7PCh. 25.5 - Prob. 25.8PCh. 25.6 - How would you use a simple extraction to separate...Ch. 25.6 - Prob. 25.10P
Ch. 25.8A - Circle the isoprene units in geranial, menthol,...Ch. 25.8B - Prob. 25.12PCh. 25.8B - Prob. 25.13PCh. 25 - Prob. 25.14SPCh. 25 - Prob. 25.15SPCh. 25 - Show how you would convert oleic acid to the...Ch. 25 - Give the general classification of each compound....Ch. 25 - Phospholipids undergo saponification much like...Ch. 25 - Prob. 25.19SPCh. 25 - Prob. 25.20SPCh. 25 - Prob. 25.21SPCh. 25 - Prob. 25.22SPCh. 25 - Prob. 25.23SPCh. 25 - The structure of limonene appears in Problem25-13....Ch. 25 - Prob. 25.25SPCh. 25 - Prob. 25.26SPCh. 25 - Prob. 25.27SPCh. 25 - Prob. 25.28SPCh. 25 - Prob. 25.29SPCh. 25 - Prob. 25.30SPCh. 25 - Prob. 25.31SPCh. 25 - Prob. 25.32SP
Knowledge Booster
Similar questions
- provide proper explanation of this question.arrow_forwardShow how to convert carboxylic acids to other functional groups, and devisemultistep syntheses using carboxylic acids as starting materials and intermediates.Explain how acid chlorides are used as activated derivatives of carboxylic acidsarrow_forward1) Nitriles are typically hydrolyzed to form what class of compounds? 2) what must one keep in mind when performing the hydrolysis of a nitrile to a carboxylic acid? 3) why are nitriles over-looked as carboxylic acid derivatives?arrow_forward
- Write the equations to show how isobutyric acid could be converted to each of the following using needed reagentsa. magnesium isobutyrateb. isobutyryl chloridec. isobutyl alcohold. ethyl isobutyratee. isobutyramidearrow_forwardLipoic acid is required by many microorganisms for proper growth. As a disulfide, it functions in the living system by catalyzing certain oxidation reactions and is reduced in the process. Write the structure of the reduction product.arrow_forwardProntosil is an antibacterial sulfa drug. Provide the intermediates, reagents, and product complete this synthesis. Ignore inorganic byproducts.arrow_forward
- What are other methods that can produce esters other than Fischer esterification? List and explain.arrow_forwardIsoamyl Acetate Synthesis One method to promote the formation of the ester is to add an excess of acetic acid. Suggest another method to shift the reaction toward ester formation.arrow_forwardPredict the product to complete the reaction.arrow_forward
arrow_back_ios
arrow_forward_ios
Recommended textbooks for you
- Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage LearningChemical Principles in the LaboratoryChemistryISBN:9781305264434Author:Emil Slowinski, Wayne C. Wolsey, Robert RossiPublisher:Brooks ColeOrganic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning
Chemistry for Today: General, Organic, and Bioche...
Chemistry
ISBN:9781305960060
Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen
Publisher:Cengage Learning
Chemical Principles in the Laboratory
Chemistry
ISBN:9781305264434
Author:Emil Slowinski, Wayne C. Wolsey, Robert Rossi
Publisher:Brooks Cole
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning