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- Draw the products formed when CH3CHC ≡ CCH2CH3 is treated with each reagent: (a) Br2(2 equiv); (b) Cl2 (1 equiv).Which of the following is an acetal? ОН ОН А) H;С—С—ОН B) H;C-Ċ-0CH; OH OCH3 С) НС—С—ОН D) H;C-c-oCH; ÓCH;Draw the products formed when p-methylaniline (p-CH3C6H4NH2) istreated with following reagent. (CH3)2C=O
- Draw the product formed when CH3CH2C=CH is treated with each of the following sets of reagents: (a) H2O, H2SO4, HgSO4; and (b) R2BH, followed by H2O2, HO−.ua U LIIUUSE une correct name tor each structure shown. [ Select) H. CH3 [ Select ] a- OH O CH) HO-E-E- -CH,-CH, CH, [ Select ) V [ Select ] CH-CH,-CH2-C-o-CH, methyl butanoate methyl carboxybutane butyl methanoate CH,-CH-NH-CH, CH, methyl butyl ester H3CN-CH3 'N' [ Select ) [ Select ) H. CH3 -OH [ Select ] CI O CH, HO-C -CH,-CH, [ Select ) ČH, ( Select ) CH,-CH, -CH2-č-o-CH, CH,-CH-NH-CH, V[ Select ] CH, 1,1-dimethylbenzne dimethyl-nitro-benzene H3C CH3 N. 1,1 dimethylcyclohexane N-methyl-2-propanamine [ Sel [ Select ] CH3-CH2-CH2-c-o-CH, CH3-CH-NH-CH; ( Select ] ČH3 H3C., -CH V [ Select ] dimethyl-nitro-benzene 1,1 dimethylcyclohexane N,N - dimethylaniline 1,1-dimethylbenzne NH, [ Select) H,C. NH, [ Select ] CH3-CH2-C-NH - CH,The key step in a reported laboratory synthesis of sativene, a hydrocarbon isolated from the mold Helminthosporium sativum, involves the following base treatment of a keto tosylate. What kind of reaction is occurring? How would you complete the synthesis?
- Thioglycolic acid, HSCH2CO2H, a substance used in depilatory agents (hair removers) has pKa = 3.42. What is the percent dissociation of thioglycolic acid in a buffer solution at pH = 3.0?Draw the product formed when pentanal (CH3CH2CH2CH2CHO) is treatedwith following reagent. With some reagents, no reaction occurs. [1] HC≡CNa; [2] H2ODraw the products formed when A is treated with each reagent: (a) H2 + Pd-C; (b) mCPBA; (c) PCC; (d) CrO3, H3SO4, H2O; (e) Sharpless reagent with (+)-DET.