Why do alkenes undergo electrophilic addition reactions ?

Alkenes and alkynes are unsaturated hydrocarbons and undergo electrophilic addition reactions. In alkenes, the addition occurs in one step while in alkynes the addition occurs in two steps. Alkenes show geometrical isomerism but alkynes do not. Alkynes are more acidic than alkenes which are more acidic than alkanes. Both alkenes and alkynes can be prepared by the electrolysis of sodium or potassium salts of carboxylic acids. Write the major product of the reaction : (CH_(3))_(3)C-CH=CH_(2)overset(HBr)to

Alkenes and alkynes are unsaturated hydrocarbons and undergo electrophilic addition reactions. In alkenes, the addition occurs in one step while in alkynes the addition occurs in two steps. Alkenes show geometrical isomerism but alkynes do not. Alkynes are more acidic than alkenes which are more acidic than alkanes. Both alkenes and alkynes can be prepared by the electrolysis of sodium or potassium salts of carboxylic acids. Write the major product of the following reaction : CH_(3)C=CH+H_(2)O overset(Hg^(24))underset("dil.H"_(2)SO_(4))to

Alkenes and alkynes are unsaturated hydrocarbons and undergo electrophilic addition reactions. In alkenes, the addition occurs in one step while in alkynes the addition occurs in two steps. Alkenes show geometrical isomerism but alkynes do not. Alkynes are more acidic than alkenes which are more acidic than alkanes. Both alkenes and alkynes can be prepared by the electrolysis of sodium or potassium salts of carboxylic acids. Which of the following molecule can exhibit geometrical isomerism ? 2-Methylbut-2-en-1-ol , 3-Methylbut-2-en-1-ol

Why do alkenes prefer to undergo electrophilec addition reaction while arenes prefer electrophilic substitution reactions ? Explain.

The alkenes have pi -bonds which make them highly reactive. These undergo electrophilic addition reactions, Addition of HX to unsymmetrical alkenes gives two products and follow Markovnikov rule and anti- Markovnikov rule. The addition occure through the formation of carbocation in Markovnikov rule and free radicals in anti-Markovnikov zule. The ozonolysis reaction of alkenes helps to locate the position of double bond. Name the products formed when 2-methylpropene is treated with ozone followed by Zn, H_(2)O .

The alkenes have pi -bonds which make them highly reactive. These undergo electrophilic addition reactions, Addition of HX to unsymmetrical alkenes gives two products and follow Markovnikov rule and anti- Markovnikov rule. The addition occure through the formation of carbocation in Markovnikov rule and free radicals in anti-Markovnikov zule. The ozonolysis reaction of alkenes helps to locate the position of double bond. What product is obtained when propene reacts with CI_(2) in the presence of water?

Alkenes and carbonyl compounds both contain a pi bond but alkenes show electrophilic addition reactions whereas carbonyl compounds show nucleophilic addition reactions. Explain.