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- aw the products for the following reactions showing the formation of amides. Name the 5. reactants and the products. CH Nit + Ho- Cat b) CH-CH NH looc Cat. oH -WH looc cat 6. Draw the products when each of the amides undergoes acid hydrolysis. Name the reactants and products. HCL Cty- -NH-C_Cy+ 0 HCL b) C-CH-N-&cnycy +4,0 HCL + H,0 dig30 COOH (1) 2 CH3CH₂Li (2) H3O+ H3O+ C=PPh3 H я ↑ CH3 NH2 H+, heat (lose H₂O)COOH 100 Amide tO NHCH
- 1. Lit :E 2. HCI Br2, H20 Isunepe enc toss1gwolol ert to rlose 107 (2nion S bonsdmun ed bluorde yisaeesen li ele bensdr CI 18 LICH3 HO 1emonsne+ CI H. (MCPBA) rt ol egete bns ainepssonitail elesrinye biewiols s2ogon9 (niog E E eluoslom e pelom CH3OH catalytic H2SO4Draw the organic product(s) for each of the following reactions. If there is more than one product likely indicate the major. Be sure and show any stereochemistry.y 10-Whic.g ne yo1owing compounds is theigtrongest base |(circle your angwers? wnicn Of the foilow ing compounds in the strongegt basl (circle your anower)? THN NH2 12. which Of the following compounds Possesses a 3° amine (crce all possible angwerg) ? NH
- Arrange the following compounds in decreasing order of acidity * |- CICH2CH2CH2COOH Il - CH3CH2CHCICOOH III – CH3CHCICH2COOH III > I> || O I > II > || O I > I| > II III > || >|Determine which of the following bases is strong enough to deprotonate acetonitrile (CH3CN), so that equilibrium favors the products:(a) NaH; (b) Na2CO3; (c) NaOH; (d) NaNH2; (e) NaHCO3.Using the data in Appendix C, determine which of the following bases is strong enough to deprotonate acetonitrile (CH3CN), so that equilibrium favors the products: (a) NaH; (b) Na2CO3; (c) NaOH; (d) NaNH2; (e) NaHCO3.