As we know 1° alkyl halide and polar aprotic solvent favours SN2 and 3° alkyl halide and polar protic solvent favours sn1 and E1. While 3° alkyl halide and strong base favoured E2.
A) Sn2
B )Sn2
C) E1
D) sn1
E) E1
F) E2
G) Sn2
H) sn1
I) E1
2. Predict which reactions proceeded by an SN1, SN2, El or E2 mechanism: NaOCH-CHa Br оСнCH +NaBr носH-Cнь 50° b. +...
1. For each of the following reactions, write S if it is a substitution and E if it is an elimination. Also write R for all of those that are also rearrangements. CH-Oн heat NaOCHs + HBr HG OH Nal Hо acetone NaBr +HBr 2. Predict which reactions proceeded by an SN1, SN2, El or E2 mechanism: NaOCH CH +NaBr оснCH Носн,сн, 50° +NaCl Nal DMSO, 45 Br NaOCHa +NaBr +HOCH Носн, 100° но +HI acetone, 50 HSO +HO HO,...
please answer all Chemistry 420 1. For each of the following reactions, write S if it is a substitution and E if it is an elimination. Also write R for all of those that are also rearrangements. w = 8 2. Predict which reactions proceeded by an SI, SN2. El or E2 mechanism: NHOCHCH, OCH CHg+NaBr HOCH, CH, 50° + Naci Nal DMSO, 45° NaOCH +NaBr + HOCH HOCH, 100° H2O + HI acetone, 50° HO HOSO Hy0, 120° xha...