Which of the following compounds is most acidic?
Cl-CH2-CH2-OH
C.
When electron withdrawing groups are attached at ortho or para-positions of phenol/ carboxylic acid, they increase the acidic nature.
As-NO2 is a strong electron withdrawing group. It pulls the electron density towards itself, weakens the -OH bond. Hence, increases the acidic nature.
The reaction which involves dichlorocarbene as an electrophile is
Reimer-Tiemann reaction
Kolbe's reaction
Friedel-Craft's acylation
Fittig reaction
Ethanol is converted into ethoxy ethane,
by heating excess of ethanol with conc. H2SO4 at 140°C
by heating ethanol with excess of conc. H2SO4 at 443 K
by treating with conc. H2SO4 at room temperature
by treating with conc. H2SO4 at 273 K
An organic compound X is oxidised by using acidified K2Cr2O7 solution. The product obtained reacts with phenyl hydrazine but does not answer silver mirror test. The compound X is,
2-propanol
Ethanal
Ethanol
CH3CH2CH3
Predict the product 'C' in the following series of reactions:
CH3-COOH
CH3CH(OH)C6H5
CH3CH(OH)C2H5
(CH3)2C(OH)C6H5
In the following sequence of reactions,
A CH3CH2OH
The compound A is
propane nitrile
ethane nitrile
CH3NO2
CH3NC
Which of the following is not true?
In vulcanisation, the rubber becomes harder and stronger
Natural rubber has 'trans' configuration at every double bond
Buna-S is a copolymer of butene and styrene
Natural rubber is 1, 4-polymer of isoprene
Which of the following is correct about H-bonding in DNA?
A - T; G - C
A - G; T - C
G - T; A - C
A - A; T - T