Alkyl Halides

A. Nucleophilic substitution
B. Nucleophilic addition
C. Elimination
D. both A & C

A. primary alcohol
B. secondary alcohol
C. tertiary alcohol
D. dihydric alcohol

A. formaldehyde
B. ketone
C. ethylene epoxide
D. both A & C

A. they have an electrophilic carbon
B. they have an electrophilic carbon & a good leaving group
C. they have an electrophilic carbon & a bad leaving group
D. they have a nucleophilic carbon & a good leaving group

A. E1 + E2
B. E2 + SN2
C. E1 and SN1
D. SN1 and SN2

A. primary alkyl halide
B. secondary alkyl halide
C. tertiary alkyl halide
D. all

A. propane
B. propanoic acid
C. propanal
D. propanol

A. 2 moles of ethane
B. 1 mole of ethane
C. 2 moles of butane
D. 1 mole of butane

A. CH3-X
B. (CH3)3 C-CH2 – X
C. (CH3)2 CH – X
D. (CH3)3 C – X

A. C2H5O-
B. SCN-
C. NH3
D. H3C+