B. a. The MW of the carboxylic acid above: g/mol; derivative MW: g/mol b. Assuming the carboxylic acid is the limiting reagent, calculate the theoretical yield of amide derivative your prepared (show calculations): c. Theoretical yield: d. Calculate percent yield (crude) of your amide (show calculations). %

B. a. The MW of the carboxylic acid above: g/mol; derivative MW: g/mol b. Assuming the carboxylic acid is the limiting reagent, calculate the theoretical yield of amide derivative your prepared (show calculations): c. Theoretical yield: d. Calculate percent yield (crude) of your amide (show calculations). %

Chemistry for Today: General, Organic, and Biochemistry

9th Edition

ISBN:9781305960060

Author:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen

Publisher:Spencer L. Seager, Michael R. Slabaugh, Maren S. Hansen

Chapter13: Alcohols, Phenols, And Ethers

Section: Chapter Questions

Problem 13.51E: Complete the following reactions: a. b. c.CH3SSCH2CH3+2(H)

See similar textbooks

Similar questions

Choices: A. Alkyl Halides B. Ketone C. Alcohol D. Ether E. Aromatic hydrocarbon F. Amine G. Amide H. Ester I. Carboxylic acid J. Aldehyde
1 Give an example (molecular structures) of each functional group. Use arbitrary alkyl groups (e.g., methyl, ethyl, etc.) ex. carbonate a b. C. d. e. f. 9. h. i. halohydrocarbons (for each halogen) alcohols (for primary, secondary, and tertiary) ethers aldehydes ketones carboxylic acids محمد esters amines (for primary, secondary, and tertiary) Draw the molecular structure of 4-chloro-2,5-dimethyl-3-heptanone. Draw the molecular structure of isopropyl acetate.
2. Differentiate acetic acid from hydrochloric acid in terms of. a. Boiling point b. Acidity c. Solubility in ethyl alcohol
Comparing the solubilities of the two compounds pentanoic acid and heptane,pentanoic acid_________as heptane.
Draw the complete Lewis electron dot structure for dichlorocarbene, :CCl₂. In the reaction of an alkene with dichlorocarbene, the dichlorocarbene is the: a. electrophile. b. Lewis base. The reaction of an alkene with dichlorocarbene is: a. regiospecific. b. Markovnikov. c. nucleophile. c. stereospecific. d. both b and c. d. non-Markovnikov.
What would be the theoretical and % yield ?
Compare aldehydes and ketones as to: (Use acetaldehyde and acetone as examples). A. Reaction with cone. NaOH, heated B. Reaction with phenylhydrazine
a) The F-F bond dissociation energy (BDE) is approximately 37 kcal/mol.For reference, a “normal” C-C or C-H bond has a BDE of approximately 100kcal/mol. Briefly explain why the F-F bond is much weaker than a C-C or C-H bond b) Consider the balanced equation below, where “Ph” indicates amonosubstituted benzene (“phenyl”) ring: Ph-H + F-F -> Ph-F + H-F The BDEs of the molecules involved, in kcal/mol, are as follows:Bond BDE (kcal/mol)Ph-H 112Ph-F 116H-F 136 What is the delta H for the fluorination of benzene by F2? Is the reaction favored or not? c) Why is the fluorination of benzene with F2 rarely done? For reference, thebromination of benzene with Br2 has a delta H of approximately -12 kcal/mol.
Propanenitrile undergoes acid hydrolysis to give Select one: a. propanamide. b. butanone. c. propanamine. d. propanoic acid. The formation of cyanohydrin is an example of Select one: a. Electrophilic addition b. Electrophilic substitution c. Nucleophilic addition d. Nucleophilic substitution
QUESTION 4 4. Match the following compounds with the correct CLASS: A. Alcohol H H B. Aldehyde H C C-C C C. Carboxylate salt D. Ester O-H E. Carboxylic Acid H H H. F. Methyl 2-hydroxybenzoate (common name: Methyl Salicylate) CH,CH,CH,OCCH, H3C. ONa
Give the IUPAC names of the following molecules: (aldehydes)
V. Questions 1. Correlate the number of carbon in the R group with the solubility of the acid in water.