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D The alkyl substituents are a methyl group at C 2 and two ethyl groups at C 4 and C 5 .
List the substituents in alphabetical order and the IUPAC name can be generated.
4,5-Diethyl-2-methylheptane
Note that numbers are separated by commas, and number and letters are separated
by hyphens. Finally, the final substituent and the parent name are written as one word.
Q 2.8. Write IUPAC names for the following hydrocarbons.
D
E
F
G
H
I
Q 2.9. Draw structural formulae for the following.
(a) 2,4,4-Trimethylheptane (b) 4-Ethyl-2-methylhexane
(c) 3-Ethyl-1-heptyne (d) 3,5-Dimethyl-4-hexen-1-yne
(e) 1,1-Dimethylcyclopentane (f) 1-Methyl-1,3-cyclopentadiene
(g) Triphenylmethane (h) o -Hexylisobutylbenzene
(i) 1-Ethyl-4-nitrobenzene (j) 2-Chloro-1,3,5-trinitrobenzene
Q 2.10. Draw structures for compounds that have the following features.
(a) A quaternary carbon and a secondary amine
(b) One secondary and two tertiary carbons
(c) An aldehyde bonded to a secondary carbon
(d) Two methylene and three methyl groups
(e) An isopropyl and a tertiary butyl group
(f) An alkene and a nitrile
(g) A secondary and a tertiary alkyl halide
(h) A dimethylphenyl group and a carboxylic acid
(i) An unsymmetrical ether
(j) A cyclic ester
(k) An alkyl-aryl ketone
(l) Non-aromatic with four coplanar carbon atoms.
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