Question

1. Use the template below to summarize all methods to prepare alcohols. Reagent Reaction Scheme Substrate (s) Comments Functional group of the product Mechanism (type) Stereochemical Implications Alkyl Halide hydroxide alcohol R-Br + oH — R-OH + Br® Sw2 yes, with secondary R-X. Inversion of stereochemical configuration Works for CH3-X, primary and secondary Alkyl Halide Alkene

Answer 1

Substrate Reagent Functional roup g Mecha nisn Stereochemical implication Reaction scheme COmmentS 0वपट Alky haide Hy droxlde aicohol RBr + OHR-oy te CNaon) Yes with seconday R-XInversion of Conbiguration SN Works bor CX Priay 4 secrday R AIKY hauide Hydroxlde Alcohol (Naon) Works o7 es, ও R-x Racem sation takes place. R-CIBY + OM RCO4 RICIK tBre Toxtiany AIKene Acdd +o A1coho1 AddiHon Works or No C of e g व

Hore Primany se con with hydroxfde gives 64 cohol. Back si de atack तिखर ह् र्यकेर ््टे शड /५ce ং s0 Conbiguration dary haiide undergo reaCHon inversion in takes place of tertiay a akyl haiide In Case Carboration is lormed in 1or step hen nudeophilie artaik taker place so ceopजर रबेकक घरm side. Thureore we Acohols are also ob tained rom alkKreme Alkene undrergo reaction with Water in acidl catatyk giver alco holTuis S additi on meactin carbon double bond attack o back berent get racemicpoe duct १rere water acToss carbon