Given that A = 1, 2-dibromopropane
How would you convert B into its corresponding alcohol?
Give a mechanism for the reaction
Give the structures of:
A. 1, 2-dibromopropane
B. 2-methyl-2-chloro ethane
How would you obtain A from propene? Give a mechanism for the reaction
Give the reagents and reaction conditions for the reactions I, II, III, & IV
C2H5Br ➡ CH3CH2CN ---------------------- (I)
CH3CH2CN ➡ C3H6O2 ------------- (II)
C2H5Br ➡ C2H6O ------------------------(III)
C2H6O + C3H6O2 ➡ C5H10O2 ------------ (IV)
Give the structure of any four Isomers of C5H10O2
The question below is based on the compounds A to D:
A. CH3CH2CH2NH2
B. CH3CH2CONH2
C. C6H5NH2
D. CH3CH2CO2NH4
9a. Give the reagents and conditions by which C may be converted into diazonium salt, and hence into azo-dye.
9b. Give the structure and name of the diazonium salt.
State which compound A ➡ C shows the least basic character. Explain your choice.
A. CH3CH2CH2NH2
B. CH3CH2CONH2
C. C6H5NH2
D. CH3CH2CO2NH4
Give the reagents and conditions which you would use to
(i) Prepare A from B
(ii) Convert B into ethylamine.
Give the systematic name for each of the following compounds
A. CH3CH2CH2NH2
B. CH3CH2CONH2
C. C6H5NH2
D. CH3CH2CO2NH4
State which if these compounds would react with aqueous sodium hydroxide to form ammonia.
Write an equation for one such reaction.
Benzene can be prepared from sodium benzoate by fusing sodium benzoate with sodium hydroxide. This process is called carboxylation.
What is meant by carboxylation?
Write an equation for the reaction.
The question below is based on the following compounds:
(a) CH3CH(OH)CH2CH3
(b) (CH3)3CBr
(c) CH3CH2CH2CHO
(d) CH3CH2CH=CH2
(e) HO2CCH2CH2CO2H
(i) An ester
(ii) an acetal
(i) D with Bromine
(ii) B with aqueous alkali
Write the systematic name for each of the following compounds:
(a) CH3CH(OH)CH2CH3
(b) (CH3)3CBr
(c) CH3CH2CH2CHO
(d) CH3CH2CH=CH2
(e) HO2CCH2CH2CO2H
Use letters A to E to refer to the compounds (if any) which
(i) exhibits optical Isomerism
(ii) react with concentrated sulphuric acid to form an alkene.
(iii) Polymerise under appropriate conditions