Pearson eText Organic Chemistry -- Instant Access (Pearson+)
9th Edition
ISBN: 9780135213728
Author: Leroy Wade, Jan Simek
Publisher: PEARSON+
expand_more
expand_more
format_list_bulleted
Concept explainers
Question
Chapter 11.12, Problem 11.31P
(a)
Interpretation Introduction
Interpretation:
The alcohol and the acid chloride that combines to make the given ester are to be stated.
Concept introduction:
An alcohol and an acid chloride mix together and form an ester with removal of hydrogen chloride. To neutralize the hydrogen chloride (side product), pyridine is used as a catalyst.
(b)
Interpretation Introduction
Interpretation:
The alcohol and the acid chloride that combines to make the given ester are to be stated.
Concept introduction:
An alcohol and an acid chloride mix together and form an ester with removal of hydrogen chloride. To neutralize the hydrogen chloride (side product), pyridine is used as a catalyst.
(c)
Interpretation Introduction
Interpretation:
The alcohol and the acid chloride that combines to make the given ester are to be stated.
Concept introduction:
An alcohol and an acid chloride mix together and form an ester with removal of hydrogen chloride. To neutralize the hydrogen chloride (side product), pyridine is used as a catalyst.
(d)
Interpretation Introduction
Interpretation:
The alcohol and the acid chloride that combines to make the given ester are to be stated.
Concept introduction:
An alcohol and an acid chloride mix together and form an ester with removal of hydrogen chloride. To neutralize the hydrogen chloride (side product), pyridine is used as a catalyst.
Expert Solution & Answer
Want to see the full answer?
Check out a sample textbook solution
Students have asked these similar questions
please help and i am so confused if the picture is the gc data or ir spectrum. you dont have to do everything just what you can please because i am lost and the mass of the cloves was Mass of cloves 62.299g. Mass of recovered clove oil 62.761g.
Which compound would you expect to have a higher decomposition temperature,Na2CO3 or Cs2CO3? Justify your answer, but you do not need to do any calculations.
Can I get some help drawing my arrows. I included what the final needs to look like
Chapter 11 Solutions
Pearson eText Organic Chemistry -- Instant Access (Pearson+)
Ch. 11.1 - Prob. 11.1PCh. 11.2C - Prob. 11.2PCh. 11.3 - Prob. 11.3PCh. 11.3 - Prob. 11.4PCh. 11.3 - Prob. 11.5PCh. 11.3 - Suggest the most appropriate method for each of...Ch. 11.4 - A chronic alcoholic requires a much larger dose of...Ch. 11.4 - Unlike ethylene glycol, propylene glycol...Ch. 11.5 - Predict the major products of the following...Ch. 11.5 - Show how you would convert propan-1-ol to the...
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
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
- Which of the m/z values corresponds to the base peak in the mass spectrum shown? 100 80 A. 45 B. 44 C. 29 D. 15 Intensity 20 0 10 20 30 40 B- m/z -8 50 E. 30 Which of the m/z values correspond to the molecular ion for the compound shown? A. 18 B. 82 OH C. 100 D. 102 E. 103arrow_forwardCan someone help me with drawing my arrows.arrow_forwardCan I get help drawing my arrows #2arrow_forward
- Can I get some help with my arrows? I have included what the final outcome needs to look like. #3arrow_forwardPlease explain how to calculate the pH.arrow_forwardI'm having trouble with converting lewis diagrams into VSEPR diagrams. I currently have this example of C2BrCl3 which I want to turn into a lewis structure, but I'm not sure what steps I need to do in order to do so. I have the table written down, however, there's two central atoms so what would I do? There seems to be 4 electron domains on the carbon atom and no lone pairs so it would seem like this shape would be tetrahedral. Here's what I have now. Thanks!arrow_forward
arrow_back_ios
SEE MORE QUESTIONS
arrow_forward_ios
Recommended textbooks for you
World of Chemistry, 3rd editionChemistryISBN:9781133109655Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCostePublisher:Brooks / Cole / Cengage Learning
Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning
Organic And Biological ChemistryChemistryISBN:9781305081079Author:STOKER, H. Stephen (howard Stephen)Publisher:Cengage Learning,
General, Organic, and Biological ChemistryChemistryISBN:9781285853918Author:H. Stephen StokerPublisher:Cengage Learning
Chemistry for Today: General, Organic, and Bioche...ChemistryISBN:9781305960060Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. HansenPublisher:Cengage Learning
Living By Chemistry: First Edition TextbookChemistryISBN:9781559539418Author:Angelica StacyPublisher:MAC HIGHER
World of Chemistry, 3rd edition
Chemistry
ISBN:9781133109655
Author:Steven S. Zumdahl, Susan L. Zumdahl, Donald J. DeCoste
Publisher:Brooks / Cole / Cengage Learning
Organic Chemistry: A Guided Inquiry
Chemistry
ISBN:9780618974122
Author:Andrei Straumanis
Publisher:Cengage Learning
Organic And Biological Chemistry
Chemistry
ISBN:9781305081079
Author:STOKER, H. Stephen (howard Stephen)
Publisher:Cengage Learning,
General, Organic, and Biological Chemistry
Chemistry
ISBN:9781285853918
Author:H. Stephen Stoker
Publisher: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
Living By Chemistry: First Edition Textbook
Chemistry
ISBN:9781559539418
Author:Angelica Stacy
Publisher:MAC HIGHER