Illustrate the different structural isomers of the following molecules.
1. C6H14
2. C5H11Cl
3. C7H7I
containing benzene
ring
4. C4H8O
5. C4H8O2
1. The isomers of C6H14 are;
(a) 2-methylpentane.
CH3 CH(CH3) CH3 CH3 CH3
(b) 2,3-dimethylbutane
CH3 CH(CH3) CH (CH3)
(c) 2,2-dimethylbutane
CH3 C(CH3)2 CH2 CH3
(d) n-hexane
CH3 CH2 CH2 CH2 CH2 CH3
2. The isomers of C5H11Cl are;
(a) 1-chloropentane
CH2(Cl) CH2 CH2 CH2 CH3
(b) 2-chloropentane
CH3 CH(Cl) CH2 CH2 CH3
(c) 3-chloropentane
CH3 CH2 CH(Cl) CH2 CH3
(d) 1-chloro-2-methylbutane
CH2(Cl) CH(CH3) CH2 CH3
(e) 1-chloro-3-methylbutane
CH(Cl) CH2 CH(CH3) CH3
(f) 2-chloro-3-methylbutane
CH3 CH(Cl) CH(CH3) CH3
(g) 1-chloro-2,2-dimethylpropane
CH(Cl) C(CH3)2 CH3
3. Isomers of C7H7I
(a) 1-iodo-2-methylbenzene
(b) 1-Iodo-3-methylbenzene
(c) 1-iodo-4-methylbenzene
(d) iodomethyl benzene
4. Isomers of C4H8O
(a) Butanal
CH3 CH2 CHO
(b) 2-butanone
CH3COOCH2CH3
(c)Cyclobutanol
CH2CHOHCH2CH2
(d) 1,2-epoxybutane
CH2OCHCH2CH3
(e) Cis-2,3epoxybutane
(f) trans-2,3 epoxybutane
(g) 2-buten-1-ol
Ch3CH=CHCH2OH
(h) 3-buten-1-ol
CH2=CHCH2CH2OH
5. Isomers of C4H8O2 are:
(a) N-propylmethanoate
HCOOCH(CH3)2
(b) Isopropyl formate
HCOOCH(CH3)2
(c) Ethyl acetate
CH3COOCH2CH3
(d) methyl propionate
CH3CH2COOCH3
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