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

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

Chemistry
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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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
Transcribed Image Text: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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