GENERAL,ORGANIC+BIOCHEM (LOOSELEAF)
GENERAL,ORGANIC+BIOCHEM (LOOSELEAF)
10th Edition
ISBN: 9781264035090
Author: Denniston
Publisher: MCG
bartleby

Concept explainers

bartleby

Videos

Question
Book Icon
Chapter 17, Problem 17.41QP
Interpretation Introduction

Interpretation:

An equation for the esterification of glycerol with a molecule of hexadecanoic acid, a molecule of dodecanoic acid and a molecule of decanoic acid has to be written.

Concept Introduction:

Esterification reaction: Esters are prepared by the reaction of a carboxylic acid and an alcohol molecule with the elimination of water molecule. The addition of a strong acid such as H2SO4 is used to increase the rate of reaction.

Here, the OH group is attached to the carbonyl carbon atom of the carboxylic acid is being replaced by OR' in the alcohol forming ester and water.

Addition Reaction:

  • It is a type of reaction in which two reactants adding together to form a single product.
  • It can be said as a reverse reaction of elimination reaction.
  • It is a characteristic reaction of alkane.

Hydrogenation reaction is an addition reaction in which addition of hydrogen to an unsaturated molecule occurs

Blurred answer
Students have asked these similar questions
10. Stereochemistry. Assign R/S stereochemistry for the chiral center indicated on the following compound. In order to recieve full credit, you MUST SHOW YOUR WORK! H₂N CI OH CI カー 11. () Stereochemistry. Draw all possible stereoisomers of the following compound. Assign R/S configurations for all stereoisomers and indicate the relationship between each as enantiomer, diastereomer, or meso. NH2 H HNH, -18
b) 8. Indicate whether the following carbocation rearrangements are likely to occur Please explain your rational using 10 words or less not likely to occur • The double bond is still in the Same position + Likely to oc occur WHY? -3 H3C Brave Chair Conformers. Draw the chair conformer of the following substituted cyclohexane. Peform a RING FLIP and indicate the most stable conformation and briefly explain why using 20 words or less. CI 2 -cobs ?? MUST INDICATE H -2 -2 Br EQ Cl OR AT Br H& most stable WHY? - 4
CH 12 Conformational Analysis. Draw all 6 conformers (one above each letter) of the compound below looking down the indicated bond. Write the letter of the conformer with the HIGHEST and LOWEST in energies on the lines provided. NOTE: Conformer A MUST be the specific conformer of the structure as drawn below -4 NOT HOH OH 3 Conformer A: Br OH A Samo Br H 04 Br H H3 CH₂ H anti stagere Br CH clipsed H Brott H IV H MISSING 2 -2 B C D E F X 6 Conformer with HIGHEST ENERGY: 13. (1 structure LOWEST ENERGY: Nomenclature. a) Give the systematic (IUPAC) name structure. b) Draw the corresponding to this name. HINT: Do not forget to indicate stereochemistry when applicable. a) ८८ 2 "Br {t༐B,gt)-bemn€-nehpརི་ཚ༐lnoa Parent name (noname) 4 Bromo Sub = 2-methylethyl-4 Bromo nonane b) (3R,4S)-3-chloro-4-ethyl-2,7-dimethyloctane # -2 -2

Chapter 17 Solutions

GENERAL,ORGANIC+BIOCHEM (LOOSELEAF)

Ch. 17.3 - Prob. 17.11QCh. 17.3 - Prob. 17.12QCh. 17.4 - Prob. 17.13QCh. 17.4 - What is meant by the term fused ring? Ch. 17.5 - Prob. 17.15QCh. 17.5 - Prob. 17.16QCh. 17 - Prob. 17.17QPCh. 17 - List the biological functions of lipids. Ch. 17 - In terms of solubility, explain why a diet that...Ch. 17 - Why are lipids (triglycerides) such an efficient...Ch. 17 - What is the difference between a saturated and an...Ch. 17 - Prob. 17.22QPCh. 17 - As the length of the hydrocarbon chain of...Ch. 17 - As the number of carbon-carbon double bonds in...Ch. 17 - Explain the relationship between fatty acid chain...Ch. 17 - Explain the relationship you described in the...Ch. 17 - Prob. 17.27QPCh. 17 - Prob. 17.28QPCh. 17 - Prob. 17.29QPCh. 17 - Prob. 17.30QPCh. 17 - Write an equation for the esterification of...Ch. 17 - Prob. 17.32QPCh. 17 - Prob. 17.33QPCh. 17 - Write an equation for the acid hydrolysis of a...Ch. 17 - Prob. 17.35QPCh. 17 - Prob. 17.36QPCh. 17 - Using line formulas, write an equation for the...Ch. 17 - Using line formulas, write an equation for the...Ch. 17 - Write an equation for the base-catalyzed...Ch. 17 - Prob. 17.40QPCh. 17 - Write an equation for the esterification of...Ch. 17 - Prob. 17.42QPCh. 17 - Prob. 17.43QPCh. 17 - Prob. 17.44QPCh. 17 - Prob. 17.45QPCh. 17 - Prob. 17.46QPCh. 17 - Prob. 17.47QPCh. 17 - Prob. 17.48QPCh. 17 - What do the terms omega-3 and omega-6 indicate...Ch. 17 - Prob. 17.50QPCh. 17 - Prob. 17.51QPCh. 17 - Prob. 17.52QPCh. 17 - Prob. 17.53QPCh. 17 - Prob. 17.54QPCh. 17 - Prob. 17.55QPCh. 17 - Prob. 17.56QPCh. 17 - Prob. 17.57QPCh. 17 - Define the term phosphatidate. Ch. 17 - Prob. 17.59QPCh. 17 - Prob. 17.60QPCh. 17 - Prob. 17.61QPCh. 17 - Prob. 17.62QPCh. 17 - Prob. 17.63QPCh. 17 - Prob. 17.64QPCh. 17 - Prob. 17.65QPCh. 17 - Prob. 17.66QPCh. 17 - Prob. 17.67QPCh. 17 - Prob. 17.68QPCh. 17 - Prob. 17.69QPCh. 17 - Prob. 17.70QPCh. 17 - Prob. 17.71QPCh. 17 - Prob. 17.72QPCh. 17 - Prob. 17.75QPCh. 17 - Prob. 17.78QPCh. 17 - Prob. 17.79QPCh. 17 - Prob. 17.80QPCh. 17 - Prob. 17.85QPCh. 17 - Prob. 17.86QPCh. 17 - Prob. 17.87QPCh. 17 - Prob. 17.88QPCh. 17 - Prob. 17.89QPCh. 17 - Prob. 17.90QPCh. 17 - Prob. 17.91QPCh. 17 - Prob. 17.92QPCh. 17 - Prob. 17.93QPCh. 17 - Prob. 17.94QPCh. 17 - Prob. 17.95QPCh. 17 - Prob. 17.96QPCh. 17 - Prob. 17.97QPCh. 17 - Prob. 17.98QPCh. 17 - Prob. 17.99QPCh. 17 - Prob. 17.100QPCh. 17 - Prob. 17.101QPCh. 17 - Prob. 17.103QPCh. 17 - What is the function of unsaturation in the...Ch. 17 - Prob. 1MCPCh. 17 - Prob. 2MCPCh. 17 - Prob. 3MCPCh. 17 - Prob. 5MCPCh. 17 - Prob. 6MCPCh. 17 - Prob. 7MCPCh. 17 - “Cholesterol is bad and should be eliminated from...Ch. 17 - Prob. 9MCPCh. 17 - When a plant becomes cold-adapted, the composition...
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
Chemistry
Chemistry
ISBN:9781305957404
Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste
Publisher:Cengage Learning
Text book image
Chemistry
Chemistry
ISBN:9781259911156
Author:Raymond Chang Dr., Jason Overby Professor
Publisher:McGraw-Hill Education
Text book image
Principles of Instrumental Analysis
Chemistry
ISBN:9781305577213
Author:Douglas A. Skoog, F. James Holler, Stanley R. Crouch
Publisher:Cengage Learning
Text book image
Organic Chemistry
Chemistry
ISBN:9780078021558
Author:Janice Gorzynski Smith Dr.
Publisher:McGraw-Hill Education
Text book image
Chemistry: Principles and Reactions
Chemistry
ISBN:9781305079373
Author:William L. Masterton, Cecile N. Hurley
Publisher:Cengage Learning
Text book image
Elementary Principles of Chemical Processes, Bind...
Chemistry
ISBN:9781118431221
Author:Richard M. Felder, Ronald W. Rousseau, Lisa G. Bullard
Publisher:WILEY
Lipids - Fatty Acids, Triglycerides, Phospholipids, Terpenes, Waxes, Eicosanoids; Author: The Organic Chemistry Tutor;https://www.youtube.com/watch?v=7dmoH5dAvpY;License: Standard YouTube License, CC-BY