Anisole is the product obtained from phenol by the reaction known

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 Multiple Choice QuestionsMultiple Choice Questions

501.

When p-nitrobromobenzene reacts with sodium ethoxide, the product obtained is

  • p-nitroanisole

  • ethyl phenyl ether

  • p-nitrophenetole

  • no reaction occurs


502.

Hydroboration oxidation of 4-methyl octene would give

  • 4-methyl octanol

  • 2-methyl decane

  • 4-methyl heptanol

  • 4-methyl-2-octanone


503.

When ethyl alcohol is heated with conc. H2SO4, the product obtained is

  • CH3COOC2H5

  • C2H2

  • C2H6

  • C2H4


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504.

Anisole is the product obtained from phenol by the reaction known as

  • coupling

  • etherification

  • oxidation

  • esterification


B.

etherification

In presence of NaOH or KOH, phenol reacts with alkyl halide and gives phenolic ether (C6H5OR).

C6H5OH + NaOH -H2O C6H5O- Na -NaXRX C6H5 -O-RVapour of C6H5OH  and CH3OH, with red hot ThO2(thoria) give anisole (phenolic ether).C6H5OH + CH3OH ThO2 C6H5OCH3 + H2O


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505.

The epoxide ring consists of which of the following

  • three membered ring with two carbon and one oxygen

  • four membered ring with three carbon and one oxygen

  • five membered ring with four carbon and one oxygen

  • six membered ring with five carbon and one oxygen


506.

In the Grignard reaction, which metal forms an organometallic bond?

  • Sodium

  • Titanium

  • Magnesium

  • Palladium


507.

Phenol is more acidic than :

  • p-chlorophenol

  • p-nitrophenol

  • o-nitrophenol

  • ethanol


508.

Trans esterification is the process of :

  • conversion of an aliphatic acid to ester

  • conversion of an aromatic acid to ester

  • conversion of one ester to another ester

  • conversion of an ester into its components namely acid and alcohol


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509.

Phenols are more acidic than alcohols because

  • phenoxide ion is stabilised by resonance

  • phenols are more soluble in polar solvents

  • phenoxides ions do not exhibit resonance

  • alcohols do not lose H atoms at all


510.

  is the anhydride of 

  • 1, 2-butane diol

  • 2, 2-butane diol

  • 2, 3-butane diol

  • 1, 1-butane diol


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