Question

I need help with question 2! thanks

------ UU UU LUU JUUSULULULILULUULIS di laucicu 15 Syl (substitution, nucleophilic, unimolecular) and Sy2 (substitution, nucleophilic, bimolecular). Tertiary alcohols follow the Snl route, primary alcohols follow the Sy2 route, and secondary alcohols can follow either path. Under acidic conditions, the mechanism (Figure 1) of the Sp1 reaction involves rapid protonation of the alcohol, followed by the loss of water as the rate-determining step. This generates a relatively stable carbocation which is then attacked by the halide ion to form the alkyl halide. Sul reactions are favored by tertiary alcohols because they tend to form more stable carbocations. CH3 CH3 CH3 HCN HC TOH н,с" сі HEC HC нас HCC Figure 1 Conversion of t-butanol into t-butyl chloride by an Syl mechanism The product will be verified by gas chromatography by comparing the chromatograms of the 1 1 . 1.1 dard

Answer 1

2e11 dest Butyl chlandle mell eitn lent-butanal give 1mole 74.3 lod BedylCHaid . 4.01 92.5 -11,3 lut-butanal 1.97 gm heuld gire 1-bufanel Chlosele t- butgl 4.97 1