Bicyclo [2.4.0] octan - 3 - ol
Bicyclo [4.2.0] octan - 3 - ol
Bicyclo [2.2.2] octan - 3 - ol
Bicyclo [4.2.0] octan - 6 - ol
.Suggest a mechanism for the reaction
)(-)-2-bromaooctane when treated with aqueous NaOH produces (+)-octan-2-ol
Write structures of the compounds whose IUPAC names are as follows. (a). 2-methylbutan-2-ol
(b). 1-phenylpropan-2-ol
(c). 3,5-dimethylhexane-1,3,5-triol
(d). 2,3-diethylphenol
(e). 1-ethoxypropane
(f). 2-ethoxy-3-methylpentane
(g). Cyclohexylmethanol
(h). 3-cyclohexylpentan-3-ol
(i). Cyclopent-3-en-1-ol
(j). 3-chloromethylpentan-1-ol
Arrange the following compounds in increasing order of boiling point. Propan - 1 - ol, butan - 1 - ol, butan - 2 - ol, pentan - 1 - ol (a) Propan-1-ol, butan-2-ol, butan - 1 - ol, pentan-1-o| (b) Propan-1-ol, butan - 1 - ol, butan-2-ol, pentan-1-ol (c) Propan-1-ol, butan-2-ol, butan-1-ol, pentan-1-ol (d) Propan-1-ol, butan-1-ol, butan-2-ol, pentan-1-ol
Write structures of the compounds whose IUPAC names are as follows:
(i) 2-Methylbutan-2-ol
(ii) 1-Phenylpropan-2-ol
(iii) 3,5-Dimethylhexane −1, 3, 5-triol
(iv) 2,3 − Diethylphenol
(v) 1 − Ethoxypropane
(vi) 2-Ethoxy-3-methylpentane
(vii) Cyclohexylmethanol
(viii) 3-Cyclohexylpentan-3-ol
(ix) Cyclopent-3-en-1-ol
(x) 3-Chloromethylpentan-1-ol.