- An SN2 reaction:
RC C − C Br
R'
HH
CH 2 R'
Na+
substitution
nucleophilic
SN 2
RC C +NaBr
Sodium
alkynide
1 o Alkyl
halide
- This synthesis fails when secondary or tertiary halides are used because the
alkynide ion acts as a base rather than as a nucleophile, and the major results is an
E2 elimination.
RC C −
C Br
C
R''
H
H R' H
H
E2 RC C + R'CH CHR'' + Br
−
2 o Alkyl halide
7.13 HYDROGENATION OF ALKENES
- Catalytic hydrogenation (an addition reaction):
- One atom of hydrogen adds to each carbon of the double bond.
- Without a catalyst the reaction does not take place at an appreciable rate.
CH 2 =CH 2 + H 2
25 oC
Ni, PdorPt CH
3 –CH 3
CH 3 CH=CH 2 + H 2 Ni, P 25 doCorPt CH 3 CH 2 –CH 3
- Saturated compounds:
- Unsaturated compounds:
- The process of adding hydrogen to an alkene is a reduction.