6.1flashcards
1
Q
Evidence for the delocalised electron structure
A
- X-ray diffraction evidence for bond length
- hydrogenation less exothermic
-undergoes substitution not addition like ethene
2
Q
Br and benzene
A
-AlCL3 used or FeBr3
-febr4- formed + Br+( electrophiles= positive charge)
-Febr4- and H+= Hbr and feBR3 to reform the catalyst
3
Q
Alkylation
A
-haloalkane and a halogen carrier
4
Q
Acylation
A
- Acyl chloride used
5
Q
Nitration of benzene
A
- HNO3 + H2SO4
-H2S04=N02+ + H20
-keep below 55 degrees for nitration
6
Q
Electron donating
A
-OH and NH2
7
Q
Electron withdrawing
A
- N02
8
Q
Phenol and bromine
A
- decolorisation
9
Q
Phenol and nitric acid
A
- 2-nitrophenol or 4-nitrophenol
10
Q
Phenol and NaOH
A
-sodium phenoxide and water
11
Q
Reduction of aldehydes and ketones
A
- Nabr4
12
Q
Hydrogen cyanide
A
- forms a hydroxynitrile
- two hydrogen used because intermediate if formed
13
Q
Carboxylic acid naming
A
- and -oic acid to the name of the longest alkane chain
14
Q
Carboxylic acid and metals
A
- salt and hydrogen gas
15
Q
Carboxylic acid and carbonate
A
- salt,carbon dioxide and water