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 Multiple Choice QuestionsShort Answer Type

161.

Write IUPAC names of the products obtained by the ozonolysis of the following compounds:
2-Ethylbut-l-ene

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162.

Write IUPAC names of the products obtained by the ozonolysis of the following compounds:
1-Phenylbut-1-ene

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163.

An alkene upon ozonolysis gives two isomeric compounds with molecular formula C3H6O. Write the structure of the compounds and also of the alkene.

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164.

An alkene 'A' on ozonolysis gives a mixture of ethanal and pentan-3-one.  Write structure and IUPAC name of 'A'.

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 Multiple Choice QuestionsLong Answer Type

165.

An alkene ‘A’ contains three C-C eight C-H bonds, one C - C straight pi bond. ‘A’ on ozonolysis gives two moles of an aldehyde of molar mass 44 amu. Write the IUPAC name of ‘A’. 

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 Multiple Choice QuestionsShort Answer Type

166.

Propanal and pentan-3-one are the ozonolysis products of an alkene? What is the structural formula of the alkene?

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167.

An alkene with molecular formula C7H14 gives propanone and butanal on ozonolysis. Write the structural formula.

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 Multiple Choice QuestionsLong Answer Type

168.

How does propene react with:
(i) Hydrogen  
(ii) Bromine
(iii) Water in the presence of mineral acid
(iv) Chlorine water (or hypochlorus acid)?

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169. Discuss in brief the oxidation reaction of alkenes.


Different products are formed depending upon the nature of the oxidising agent.

(i) Using alkaline potassium permanganate solution (Baeyer’s reagent): Alkenes react with a cold dilute alkaline solution of KMnO4 to produce diols.

The pink colour of KMnO4 gets discharged and this reaction is known as Bayer's test for the detection of unsaturation in a compound.

(ii) Using hot KMnO4: Different products are formed depending upon the structure of alkene. In such reactions, the cleavage of C = C bond occurs.
In terminal alkenes: One of the product is always methanoic acid which is further oxidised to form CO2 and H2O.


Note:= CH2 gets oxidised to CO2 and H2O.
In non-terminal alkenes. The products are carboxylic acids and/or ketones depending upon the nature of alkene.



(iii) Using hydrogen peroxide (H2O2). Alkenes react with hydrogen peroxide to form diols.


(iv) Using air in the presence of silver as a catalyst at 525-675 K. Ethylene forms ethylene oxide.



(v) Combustion. When burnt in air or oxygen, alkenes form carbon dioxide and water.



The reaction is highly exothermic in nature and the heat evolved is used for welding purposes.

 

 




 







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 Multiple Choice QuestionsShort Answer Type

170. Write structures of all the alkene which on hydrogenation give 2-methyl butane. 
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