A polymeric organic compound has formula `(C_(6)H_(3))(C_(8)H_(8))_(n)Br_(3)`. If it contains `7.68%` bromine, then the value of `n` will be [approximate]
(Atomic mass of `Br=80U`)

Write the isomers of the compound having formula C_(4)H_(9)Br .

Find compound with formula C_(4)H_(8)Br_(2) How many structure of (X) are possible?

A polystryrene, having formula Br_(3) C_(6) H_(2) (C_(8) H_(8))_(n) , was perpared heating styrene with tribromobenzoyl peroxide in the absence of air. If it was found to contain 10.46% bromine by weight, find the value of n .

A compound with molecular formula C_(8)H_(14) , contains 12 secondary and two tertiary H atoms. The compound is :

C_(6)H_(5)CH_(3) overset(Br_(2)//FeBr_(3))(to) the reaction is called

The compound [CoCI_(3)I(C_(5)H_(5)N)_(2)] Br will show the chemical test for which of the following ions? .

A compound X of formula C_(3)H_(8)O yields a compound C_(3)H_(6)O , on oxidation. To which of the following classes of compounds could X being

The structure of the compound with molecular formula C_(6)H_(12) that has only 2^(@) H atoms is:

An optically active compound A (assume dextrorotatory) has the molecular formula C_(7)H_(11)Br . A reacts with hydrogen bromide, in the absence of peroxides to yield isomeric products, B and C, with the molecular formula C_(7)H_(12)Br_(2) . Compound B is optically active, C is not. Treating B with 1 mol of potassium butoxide yields (+)-A . Treating C with 1 mol of potassium tert-butoxide yields (+-)-A . Treating A with potassium tert-butoxide yields D(C_(7)H_(10)) . Subjecting 1 mol of D to ozonolysis followed by treatement with zinc and acetic acid yields 2 moles of formaldehyde and 1 mole of 1,3-cyclopentanedione. The optically active compound 'A' is

An optically active compound A (assume dextrorotatory) has the molecular formula C_(7)H_(11)Br . A reacts with hydrogen bromide, in the absence of peroxides to yield isomeric products, B and C, with the molecular formula C_(7)H_(12)Br_(2) . Compound B is optically active, C is not. Treating B with 1 mol of potassium butoxide yields (+)-A . Treating C with 1 mol of potassium tert-butoxide yields (+-)-A . Treating A with potassium tert-butoxide yields D(C_(7)H_(10)) . Subjecting 1 mol of D to ozonolysis followed by treatement with zinc and acetic acid yields 2 moles of formaldehyde and 1 mole of 1,3-cyclopentanedione. The compound 'B' is: