Electrophilic Substitution Reactions of Haloarenes
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State effective atomic number(EAN) rule.
- 2, 4, 6−Trinitrophenol
- o-Nitrophenol
- p-Nitrophenol
- Nitrobenzene
Why Paras product is major and not ortho?
What is the correct sequence of reagents used for converting Nitrobenzene into m-dibromobenzene?
What happens when Benzene reacts with Bromine water?
The product D is:
- C6H5NHOH
- C6H5NHCH2CH3
- C6H5CH2NH2
- C6H5CH2OH
Conversion of chlorobenzene to a mixture of 2-chloroacetophenone and 4-chloroacetophenone Is an example of
Elimination reaction
Condensation reaction
Nucleophilic ring substitution
Electrophilic ring substitution
Which of the following is intermediate in Sandmeyer's reaction?
Diazonium salt
Nitronium ion
Ammonium salt
Hydronium ion
Which reagent (A) is used for the following given conversion?
high pressure
Molybdenum Oxide
Manganese Acetate
Potassium Permanganate
Reaction of alkyl halides with ammonia to form a mixture of primary, secondary and tertiary amine is:
Substitution
Addition
Ammonolysis
Elimination
- HCHO
- None of these
Potassium chlorate on heating gives potassium chloride and oxygen.
- True
- False
the carbon-halogen bond has got to be broken because that gets easier as you go from fluoride to chloride to bromide to iodide, the compounds get more reactive in that order. Why then does the boiling point also increase shouldn't they decrease if its easier to break the bonds like for there reactivity.
- benzenehexachloride
- chlorobenzene
- tetrachlorobenzene
- trichlorobenzene
- Polar protic solvent increases reactivity
- Good leaving group favours the reation
- Reaction proceeds via carbocation intermediates
- Strong base is preferred for abstraction of proton
On mixing a certain alkane with chlorine and irradiating it with ultraviolet light it forms only one monochloroalkane. The alkane is:
Propane
Pentane
Isopentane
Neopentane
Method of preparation of haloarenes by electrophilic substitution reaction
When thiosulphate ion is oxidised by iodine, which one of the following ion is produced