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Give the structures of the alkene (C4H8)...

Give the structures of the alkene `(C_4H_8)` which adds on HBr in the presence and in the absence of peroxide to give the same product , `C_4H_9Br`

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To solve the problem of identifying the structures of the alkene \(C_4H_8\) that adds HBr in both the presence and absence of peroxide to yield the same product \(C_4H_9Br\), we can follow these steps: ### Step 1: Determine the Possible Structures of \(C_4H_8\) The molecular formula \(C_4H_8\) indicates that there is one degree of unsaturation (double bond). The possible structures for alkenes with four carbon atoms include: 1. 1-butene (CH2=CH-CH2-CH3) 2. 2-butene (CH3-CH=CH-CH3) 3. Cyclobutane (not considered here as it does not fit the alkene definition) ...
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a. Write the products of the reductive and oxidative ozonolyses of mesitylene. b. Give the structure of the alkene (C_(4)H_(8)) which when treated with dil. H_(2)SO_(4) give C_(4)H_(10)O , which is non - resolvable. c. Give the structure of the alkane (C_(4)H_(8)) which adds HBr in the presence and absence of peroxide to give the same product C_(4)H_(9)Br. d. Arrange the following in the decreasing order of their reactivity towards alkenes : i. HCI,ii.HBr, iii. HI,iv. HF.

Give the structures of (A),(B) and (C)( explanation is not required ). i. (A)(C_(4)H_(8)) that adds on HBr in the presence and in the absence of peroxide to give the same product, C_(4)H_(9)Br . ii. (B)(C_(4)H_(8)), which when treated with H_(2)O //H_(2)SO_(4) gives C_(4)H_(10)O that cannot be resolves into optical isomers. iii. (C)(C_(6)H_(12), an optically active hydrocarbon which on catalytic hydrogenation gives an optically inactive compound, C_(6)H_(14))

Give the structures of A & B (explanation are not required) (i) A(C_4 H_8) which adds on HBr in the presence and in the absence of peroxide to give same product. (ii) B(C_4 H_8) which when treated with H_2 O //H_2 SO_4 gives C_4 H_(10)O which cannot be resolved into optical

The alkene that will give the same product with HBr in the presence as well as in the presence of peroxide is

Give the structure of the major organic products obtained from 3-methyl-2-pentene under HBr in the presence of peroxide.

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