Question

a Suggest an explanation for the fact that 1-methylcyclopropene is some 42 kJImol 140 (0 molo less stable than methylenecyclopropane. CH is less stable than CH2 Methylenecyclopropane l-Methylcyclopropene b. on the basis of your answer to part (a, compare the expected stability of 3-methylcyclopropene with that of 1-methylcyclopropene and that of methylenecyclopropane.
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Answer #1

a) 1-Methylcyclopropene” has two sp2- hybridized carbons in a three-membered ring which causes more angular strain as compared to angular strain caused by only one sp2- hybridized carbons in a three-membered ring of “Methylenecyclopropane"
Hence, 1-Methylcyclopropene has more angle strain than methylenecyclopropane which results in lower stability of 1-methylcycloprene than methylenecyclopropane.

b) 1-methylcycloprene is more stbale than 3-methyl cyclopropene becuause the electronegative sp2 hybridized carbon atom in the former is attached to - CH3 group which due to its +I effect will donate its electron density to sp2 carbon thus making it more stable than the later.

Where as 3-methyl cyclopropene is less stable than methylenecyclopropane because of higher angular strain in the former.

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