( +2) 2-methylbutan-1-ol (-) 2-methylbutan -1- ol have different values for which property?
Boiling point
Relative density
Refractive index
Specific rotation
D.
Specific rotation
( +) 2-methyl butan-1-ol and (-) 2-methyl butan-1-ol are enantiomer. Enantiomers are non-superimposable mirror images of each other hence, are optically active.
The optical activity of a compound can be confirmed by the value of specific rotation. It is defined as the rotation produced by solution of 10 cm length and unit concentration (1 g/ mL) for the given λ of light at the given temperature.
375 mg of an alcohol reacts with required amount of methyl magnesium bromide and releases 140 mL of methane gas at STP. The alcohol is
ethanol
n-butanol
methanol
n-propanol
D.
n-propanol
The required reaction is
Moles of CH4(n) at STP = = 0.00625 moles
Here, -CH3 of CH3MgBr combines with H-atom of R-OH to give CH4.
n(CH4) = n(R-OH)
Also, n = CnH2n+1.OH
Thus, 12n + 2n + 1 + 17 = 60 ( OH = 16 + 1 = 17)
14n = 60 - 18 = 42
n = 3
Hence, alcohol is n-propanol (C3H7OH).
Phenol is a highly corrosive substance, but it 0.2 percent solution is used as
Antibiotic
Antiseptic
Disinfectant
Antihistamine
B.
Antiseptic
0.2% phenol solution is used as an antiseptic solution.
The compound that would produce a nauseating smell/ odour with a hot mixture of chloroform and ethanolic potassium hydroxide is
PhCONH2
PhNHCH3
PhNH2
PhOH
C.
PhNH2
When primary amine reacts with chloroform and ethanolic potassium hydroxide, they produce isocyamides as main product. The reaction is also known as carbylamine reaction.
Ph-NH2 Ph.N → C
The main product (P) is
C6H5OC2H5
C2H5OC2H5
C6H5OC6H5
C6H5.I
B.
C2H5OC2H5
Since, C6H5O- is a weaker nucelophile than C2H5O-, therefore, the stronger nucleophile, i.e. C2H5O- will attack on C2H5I to give diethyl ether.
(i) C6H5OH + C2H5O- → C6H5O- + C2H5OH
(ii) C2H5O- + CH3.CH2.I → CH3CH2-O-CH2CH3
Name of the following reaction is
Reimer-Tiemann
Kolbe-Schmitt
Cannizzaro
Gattermann
B.
Kolbe-Schmitt
The given reaction is known as Kolbe-Schmidt reaction. It is used to get salicylic acid.
The order of reactivity of the following alcohols is
1 > 2 > 3 > 4
1 > 3 > 2 > 4
4 > 3 > 2 > 1
4 > 3 > 1 > 2
C.
4 > 3 > 2 > 1
The order of reactivity depends on the stability of the carbo cations of the respective species. The carbocations formed are
F.CH2.H.CH3, FCH2.CH2H.CH3
CH3.H.CH3 and Ph.H2
The stability order of carb-cation is
PhH2 > CH3.H.CH3 > F.CH2.CH2.H.CH3 > F.CH2.CH2.H.CH3 > FCH2H.CH3
Hence, order of reactivity follows the order (4) > (3) > (2) > (1)
Which of the following compound (s) will give butanone on oxidation with alkaline KMnO4 solution?
Butan-1-ol
Butan-2-ol
Both (a) and (b)
None of the above
B.
Butan-2-ol
Alkaline KMnO4 is a strong oxidising agent. It oxidises primary alcohols to aldehyde and secondary alochols to ketones.
(i)
(ii)