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
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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. two
B. three
C. one
D. four
A. Zn / HCI
B. SOCl2 / Pyridine
C. PCI3
D. PCI5
A. Nucleophilic substitution
B. Nucleophilic addition
C. Elimination
D. both A & C
A. R-F
B. R-C
C. R-Br
D. R-I
A. Dows process
B. Friedel & Craft acylation
C. Friedel & Craft alkylation
D. Clemmenson reduction
A. C2H5O-
B. SCN-
C. NH3
D. H3C+
A. Flouride ion
B. Bromide ion
C. Chloride ion
D. Iodide ion
Submitted by: Safeullah Bullo
A. Covalent halides
B. Electronegative halides
C. Polymeric halides
D. Polymeric hydrides
A. alkyl halides
B. alkyl amine
C. alkanes
D. alkynes
A. CH3-X
B. (CH3)3 C-CH2 – X
C. (CH3)2 CH – X
D. (CH3)3 C – X
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