Please answer item number 14 only. 1. Draw the structure of the organic product/s when:1. propanal reacts with ammoniacal AgNO, (Tollens' reagent)2. 3-methylbutanal forms a cyanohydrin3. 4-methyl-2-pentanone reacts with Grignard reagent, CH3CH₂MgBr4. 2-methylhexanal reacts with 2 moles of ethanol in dry acid5. two moles of phenylacetaldehyde undergo condensation to give an aldol6. the product of no.5 undergoes dehydration7.D-arabinose reacts with dilute nitric acid with heating8. benzoic acid reacts with excess isopropyl alcohol and acid catalyst9. propanoic anhydride reacts with ammonia10. ethyl benzoate undergoes acid catalyzed hydrolysis11. two moles of ethyl phenylacetate undergo condensation to give a beta-keto ester.12. a trimyristin undergoes hydrogenolysis13. p-nitroaniline reacts with NaNO₂/HCI at 0°C14. product of no. 13 reacts with CuCN/KCNHO-H-OH-OHCH₂OHD-arabinoseH-H-CH₂-C-Hphenylacetaldehyde11H₂C-O-CO11HC-0-C.L iH₂C-O-C.-CH₂-C-OCH₂CH3ethyl phenylacetatetrimyristin

At first, we start with question no 13, because product of question no 13 is essential for question…

Answered: 13. p-nitroaniline reacts with…

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Chemistry

13. p-nitroaniline reacts with NaNO₂/HCI at 0°C 14. product of no. 13 reacts with CuCN/KCN

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

Chapter15: Carboxylic Acids And Esters

Section: Chapter Questions

Problem 15.69E

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Question

Please answer item number 14 only.

1. Draw the structure of the organic product/s when:
1. propanal reacts with ammoniacal AgNO, (Tollens' reagent)
2. 3-methylbutanal forms a cyanohydrin
3. 4-methyl-2-pentanone reacts with Grignard reagent, CH3CH₂MgBr
4. 2-methylhexanal reacts with 2 moles of ethanol in dry acid
5. two moles of phenylacetaldehyde undergo condensation to give an aldol
6. the product of no.5 undergoes dehydration
7.
D-arabinose reacts with dilute nitric acid with heating
8. benzoic acid reacts with excess isopropyl alcohol and acid catalyst
9. propanoic anhydride reacts with ammonia
10. ethyl benzoate undergoes acid catalyzed hydrolysis
11. two moles of ethyl phenylacetate undergo condensation to give a beta-keto ester.
12. a trimyristin undergoes hydrogenolysis
13. p-nitroaniline reacts with NaNO₂/HCI at 0°C
14. product of no. 13 reacts with CuCN/KCN
HO
-H
-OH
-OH
CH₂OH
D-arabinose
H-
H
-CH₂-C-H
phenylacetaldehyde
11
H₂C-O-C
O
11
HC-0-C.
L i
H₂C-O-C.
-CH₂-C-OCH₂CH3
ethyl phenylacetate
trimyristin

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