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- Devise at least three different methods to prepare N-methylbenzylamine (PhCH2NHCH3) from benzene, any one-carbon organic compounds, and any required reagents.Identify the organic functional groups and reaction type for the following reaction.Please include everything including the letter and the answers.The reactant is a(n)a. amideb. aldehydec. alcohold. carboxylic acide. esterf. ketoneThe product is a(n)a. carboxlyate ionb. ammonium ionc. alcohold. carboxylic acide. ketonef. aldehydeThe reaction type isa. hydrationb. esterificationc. hydrolysis (in acid)d. hydrolysis (in base)e. amide synthesisf. amide synthesisg. dehydrationh. acid baseDraw the product formed when phenylacetic acid (C6H5CH2COOH) istreated with following reagent. With some reagents, no reaction occurs. SOCl2
- Draw the product formed when phenylacetic acid (C6H5CH2COOH) istreated with following reagent. With some reagents, no reaction occurs. CH3NH2, DCCDescribe six way to prepare to 1-pentanamine and write two ways reaction routrs to obtain 1-pentene from the two way to prepare 1-pentanamineIdentify the lettered compounds in each reaction sequence.Draw the product formed when phenylacetonitrile (C6H5CH2CN) istreated with below reagent. H2O, −OH
- (a) Write a suitable chemical equation to complete each of the following transformations :(i) Butan-l-ol to butanoic acid(it) 4-Methylacetophenone to benzene-1, 4-dicarboxylic acid(b) An organic compound with molecular formula C9H10O forms 2, 4-DNP derivative, reduces Tollen’sreagent and undergoes Cannizzaro’s reaction. On vigorous oxidation it gives 1, 2-benzenedicarboxylic acid. Identify the compound.Identify the organic functional groups and reaction type for the following reaction.The reactant is a(n) a. amideb. aldehydec. alcohold. carboxylic acide. esterf. ketoneThe product is a(n)a. carboxylate ionb. ammonium ionc. alcohold. carboxylic acide. ketonef. aldehydeThe reaction type isa. hydrationb. esterificationc. hydrolysis (in acid)d. hydrolysis (in base)e. amide synthesisf. amide synthesisg. dehydrationh. acid baseWhich of the following reaction or reagent does not produce an amine molecule? A. Curtius rearrangementB. Reaction of oximes with metallic sodium in ethanolC. Reaction of N-alkylphthalimide with hydrazineD. Hofmann transformationE. Wolff transformation
- synthesize each from benzene and sketch the following: H-NMR; C-NMR; MS, and IR for the compounds: 1. ortho form of aminophenol 2. meta form of salicylic acidGive the expected organic product when phenylacetic acid, PhCH2COOH, is treated with reagent Q.)CH3MgBr (one equivalent)Draw the product formed when phenylacetic acid (C6H5CH2COOH) istreated with following reagent. With some reagents, no reaction occurs. NH3 , Δ
