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Alkadienes and Cycloalkanes
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page3
Chapter


General formula of alkadienes is CnH2n–2
Preparation of alkadienes
(i) Dehydrogenation of butane


(ii) Pyrolysis of Cyclo alkenes


This reaction is known as Retro Diels – Alder reaction.
(iii) Dehydration of diols


(iv) Dehydrohalogenation by alc. KOH



(v) From HCHO




Properties of alkadienes


(a) In 1,3- Butadiene all carbons are in sp2 hybridisation.
(b) 1,3- Butadiene undergo resonance so that it undergo electrophilic addition reaction at both 1,2-and 1,4- position of molecule.
(c) In Butadiene C2 – C3 bond length is 1.48 Å which is less than C – C bond length of ethane while C1–C2 or C3 – C4 bond length is 1.37 Å which is slightly more than C = C of ethene.
(d) 1,3 - Butadiene undergo following type of reaction







(i) Electrophilic addition reaction (ii) Free radical addition reaction
(iii) Polymerisation (iv) Cyclic reaction

 

 

 
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