8:32 PM Tue Apr 11DoneModule 5: Other Functional Groups1. Naming Aldehydes Given Structure 1 pts M2. Naming Ketones Given StructureAA3. Drawing Aldehydes and Ketones Gi...1 pts4. Physical Properties of Aldehydes a... 1 pts5. Draw Products of Oxidations of Ald... 1 pts6. Draw Products of Addition of Hy...7. Write Carboxylic Acid IUPAC Na...8. Draw Carboxylic Acid Given Name10. Classify Amines12. Draw Amines from IUPAC Name1 pts9. Physical Properties of Carboxylic A... 1 pts13. Intermolecular Forces in Amines14. Physical Properties of Amines15. Naming AmidesQuestionQuestionQuestionProgress:12/15 groupsDue Apr 2 at 12:00 AM11. Draw Amines from Common Name 1 ptsFinish Assignment1 pts1 pts 2req1 pts1 pts 2req1 pts1 pts1 pts(M)(M)O(M)6 X(M)(M)(M)(M)(M)(M)(M)1 pts 2req(M)prod01-cnow-owl.cengagenow.comWhat is the IUPAC name of each of the the following?iCH3CH₂CNH₂Submit Answer[Review Topics][References]Use the References to access important values if needed for this question.0CH3CH₂CNHCH₂CHCH3CH3Retry Entire Group 8 more group attempts remainingCengage Learning | Cengage Technical SupportPreviousEmail InstructorNext94%Save and Exit

The given compounds are examples of acid amides and the detailed nomenclatures are given below.

What is the IUPAC name of each of the the following? CH₂CH₂CH₂ CH₂CH₂C Use the References to access important values if needed for this question. Submit Answer WHICHSCHICHI CH₂ Retry Entire Group 8 more group attempts remaining

What is the IUPAC name of each of the the following? CH₂CH₂CH₂ CH₂CH₂C Use the References to access important values if needed for this question. Submit Answer WHICHSCHICHI CH₂ Retry Entire Group 8 more group attempts remaining

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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i. LIAIH4 i. deprotection J ii. dehydration .CO2Me CH2=CHCOCH3 protection ii. H30* K The synthesis of K from H involves a 3-steps reaction as shown above. Hydrolysis of H followed by heating produces compound L. Give IUPAC name for L. Write the reaction mechanism involved during the heating process that brought iii. to the formation of L.
b. d. a. a 6. Draw the organic product formed for each reaction. COOH COOH A [1] LDA [2] CH3CH₂l [1] Br₂. CH3CO₂H [2] Li₂CO3. LiBr. DMF 12 (excess) TOH CN NaH Br₂ (excess) TOH + CHI3
11:42 PM Tue Apr 11 Done Module 5: Other Functional Groups 1. Naming Aldehydes Given Structure 1 pts M 2. Naming Ketones Given Structure AA 3. Drawing Aldehydes and Ketones Gi...1 pts 4. Physical Properties of Aldehydes a... 1 pts 5. Draw Products of Oxidations of Ald... 1 pts 6. Draw Products of Addition of Hy... 7. Write Carboxylic Acid IUPAC Na... 8. Draw Carboxylic Acid Given Name 10. Classify Amines 12. Draw Amines from IUPAC Name 1 pts 9. Physical Properties of Carboxylic A... 1 pts 13. Intermolecular Forces in Amines 14. Physical Properties of Amines 15. Naming Amides Question Question Question Progress: 12/15 groups Due Apr 2 at 12:00 AM 11. Draw Amines from Common Name 1 pts Finish Assignment 1 pts 1 pts 2req 1 pts 1 pts 2req 1 pts 1 pts (M) (M) 1 pts (M) 00 (M) (M) (M) (M) (M) (M) (M) 1 pts (M) E req Not Visited prod01-cnow-owl.cengagenow.com Submit Answer [Review Topics] [References] Use the References to access important values if needed for this question. What is the IUPAC…
6. Which of the following alcohols is oxidized to a ketone by chromic acid? I. II. III. I. II. OH III. OH CH₂OH 7. What are the major organic products when the following molecule is treated with ozone, and then with Zn/H2O? CH₂ Yu A. I B. II C. III D. IV E. V ,COH O IV. H-C-H IV. COOH V. 2 CH₂O CH₂OH CH₂ C-CH3 OH V. -OH Jº. n&on но- -он Y. A. I B.II C.III D.IV E. V 8. What compound results when 1-heptyne undergoes ozonolysis? A. heptanal B. 2-heptanone C. heptanoic acid D. hexanoic acid and CO2 E. 1-heptanol
51. Which of the following reactants can be used in the synthesis of 1-butanamine 1. LiAIH4 ? 2. H2O I. 2 CH3CH₂COCH₂CH3 I. П. CN Ш. A. I and II only B. II and III only C. I and III only 52. What is the major product of the following condensation reaction? A.I ОН II. NH₂ ОН 1.CH3CH2O 2. Н30 Jackson ČOCH₂CH3 CN III. ? CH3CH₂CHCHCOCH₂CH3 IV. CH3CH₂CCH₂CH₂COCH₂CH3 CH3 NH 0 V. CH₂CH₂CCHCOCH₂CH3 CH3 CH3CH₂CHCH₂CH₂COCH₂CH₂ В. ІІ С. III D. IV E. V D. I,II, and III
a. 1. Draw the MAJOR organic product(s) for the following reactions. If no reaction occurs state no reaction in the box provided. d. e b. H l LDA NaOH H3O+*, Br₂ 1. NaOEt JE 2. heat
Acetal and Hemiacetal formation: c. Acetal/hemiacetal CH 3 ty CH H3C [ a. hemiacetal H3C d. Cyclic hemiacetal Gyertych OH Esterification/Amidation: e. Fisher esterification OH + CH₂OH + H3C CH3 H OH + CH3OH H [H*] H₂SO4 H™ a. hemiacetal b.acetal + H₂O
12. Predict the products of the following reactions. HBr a. OH conc. H₂SO4 heat b. C₁ H₂C d. H CH3 OH OH H H Br₂/ heat Br NaOCH₂CH3 ethanol heat -CH3 NaOCH₂CH3 ethanol heat A HO 9. OH h. X Br f. j. OH conc. H₂PO4 heat SOCI₂ G conc. acid heat NaOCH 3 methanol heat methanol
PART 2 FOR EACH REACTION THAT FOLLOWS: 1. Name the functional groups & reactants 2. Name the reaction 3. Draw the major product K. L. M. N. P. Nall THE Q. 1. Hg(0Ac), MeOH 2. NaBH₂ O. m HO 1.9-BBN 2. NaOH, H₂O₂ OH OMe -OH Na Cr₂O H₂SO₂, H₂O PCC DCM PCC DCM IM NaOH(aq). (H₂C),CO cat. TsOH
a. b. d. 8. The following reagents/conditions are capable of selectively oxidizing a primary alcohol to an aldehyde a. Swern Oxidation, Jones Reagent (H₂CrO4), DIBAL-H, PCC b. Swern Oxidation, Jones Reagent (H₂CrO4), DIBAL-H c. Swen Oxidation, PCC d. Swern Oxidation, PCC, DIBAL-H H₂O+ 9. The acid-catalyzed hydrolysis of the epoxide drawn above will give a. A diol as a 50/50 mixture of enantiomers b. A diol as an enantiopure compound c. A diol as a meso compound d. No reaction 10. The reaction below is in equilibrium. Which of the following methods will help drive the reaction forward to form a near quantitative yield of products? Circle the entire answer and all answers that apply. OCH3 OCH₂ + H₂O + 2 CH₂OH Use a large excess of methanol Use a chiral reagent Distill off the water that is formed in the reaction Add a drying agent, such as sodium sulfate
a. b. C. d. e. type: OH type: type: OH 2 + OH TsOH cat. HÅH н Ἡ Acetal formation OH TsOH cat. SOCI₂ ܘ ܀ 1.2 equiv. NH3 2. LIAIH₂ 3. H₂O*
11. What is the major product of the following reaction?" a. b. II c. III d. IV NaOH/H₂O A (Heat) I II III IV Nal+H₂O + ???????