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out Package 2017.pdf W S LATOREMON SATENGSLANE # 3: CH 2004, 12 elimination note 3 or 2 carbon, apotic solvent) tavos cartons because of double bond stabdeeds a strong base to occur, foll Eelmination note follows Zaites k e d S NE C KOH r 1/1 f CHỊCH DOM D 16 5 V DOM C3 8 6 100% t y b 7 h u n 00 1 se of cabacanon jobbe 1 m k O 1 WILL P
Predict the products of the following reactions [label nucleophile (or base), substrate and leaving group]: SN2 Substitution [note 1° or 2° carbon, aprotic solvent] Br Br SCH₂ Br. CH₂ S1 Substitution [note 2 or 3° carbon, protic solvent]: Sulis always stepwise and always forms a carbocation intermediate. OCH3 + acetone NH₂ DCM KOH OCHS E2 elimination [note 3" or 2 carbon, aprotic solvent]: favors 3º carbons because of double bond stability; needs a strong base to occur, follows Zaitzev's rule. снон CH3OH SNZ-SNI-EZ-E1 DCM DCM
ut Package 2017.pdf 2 W S 5,1 Substitution [note 2 or 3 carbon, protic solvent) Sulis always stepwise and always forma carbocation intermediate 3 X + e FOCH 12 nation[note3 or carbon, aprctic solvent) favors carbons because of double bond stability needs a strong bine to occur, follows Zaev's de с Qo d 54 1994 KOH 11 elimination note 3ar 2 carbon, protic solvent favon 3'cartons because of carbocation it follows Zat's ne felos same path as S HUGO C CHOH DICH r DOM 5 DOM 96 5 t D.O D A (10 6 g y & 7 J 0 b V C n Bwwwwww..co 8 1 1 ( 9 k m O S (