Answer the following questions on the basis of final product.
•Number of carbon atoms be X.
•Degree of unsaturation be Y.
•Number of halogens present be Z.
• Number of oxygens present be A.
•Number of sp3 hybridized carbon be B.
Enter
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The product formed is cyclopropane. Hints: 1) For the first rxn when H+ attacks a double bond, carbocation is formed which further attacks the other double bond , forming a carbocation and Br- gets attached at that position ( Note a cyclic 6 membered ring is formed) 2) While forming 'T' from 'S' , a special type of carbocation rearrangement takes place which becomes highly stable due to "SIGMA RESONANCE" . (Cyclopropyl methyl carbocation is formed)