n-Butane on monochlorination under photochemical condition gives an optically active compound "P". "P" on further chlorination gives dichloro compounds. The number of dichloro compounds obtained (ignore stereoisomers) is :
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n-Butane on monochlorination under photochemical condition gives an optically active compound "P". "P" on further chlorination gives dichloro compounds. The number of dichloro compounds obtained (ignore stereoisomers) is :
Given below are two statements : In the light of the above statements, choose the correct answer from the options given below :
An optically active alkyl bromide C4H9Br, reacts with ethanolic KOH to form major compound [A] which reacts with bromine to give compound [B]. Compound [B] reacts with ethanolic KOH and sodamide to give compound [C]. One molecule of water adds to compound [C] on warming with mercuric sulphate and dilute sulphuric acid at 333 K to form compound [D]. The functional group in compound D will be confirmed by :
An alkane (Y) requires 8 moles of oxygen for complete combustion and on chlorination with Cl2/h , (Y) gives only one monochlorinated product (Z). The total number of primary carbon atoms in (Y) is .
For the following Friedel Craft's alkylation reaction, which of the statements are correct? [figure] Choose the correct answer from the options given below :
An alkene (X) on ozonolysis followed by reduction gives following products. H- O \|C-H (2 moles), H- O \|C- O \|C- O \|C-H, CH3- O \|C- O \|C- O \|C-CH3 The alkene (X) is :
[figure] Compound (X) is subjected to the sequence of reactions as shown above. Molar mass of the major product (Y) formed is g mol-1. (Given molar mass in g mol-1 C : 12, H : 1, O : 16 )
One mole of an alkane (x) requires 8 mole oxygen for complete combustion. Sum of number of carbon and hydrogen atoms in the alkane (x) is .
The compound (X) on (i) on heating in the presence of anhydrous AlCl3 and HCl gas gives 2,4-dimethyl pentane (ii) aromatization gives toluene and (iii) cyclisation gives methyl cyclohexane The correct name of compound (X) is:
Given below are two statements for the following reaction sequence. [figure] In the light of the above statements, choose the correct answer from the options given below :
Ph-CH=CH2 [HBr](PhCOO)2 Product Consider the above reaction Identify the correct statements. Choose the correct answer from the options given below :
The reactions which produce alcohol as the product are : Choose the correct answer from the options given below :
Consider the following compounds : [figure] Arrange these compounds in the increasing order of reactivity with nitrating mixture.
But-2-yne and hydrogen (one mole each) are separately treated with (i) Pd/C and (ii) Na/ liq. NH3 to give the products X and Y respectively. [figure] Identify the incorrect statements. Choose the correct answer from the options given below :
[figure] Identify (P)
Given below are two statements : In the light of the above statements, choose the most appropriate answer from the options given below
The cycloalkene (X) on bromination consumes one mole of bromine per mole of (X) and gives the product (Y) in which C : Br ratio is 3:1. The percentage of bromine in the product (Y) is %. (Nearest integer) (Given : molar mass in g mol-1 H : 1, C : 12, O : 16, Br : 80)
Consider the following reaction : [figure] The product Y formed is :
The dibromo compound [P] (molecular formula: C9H10Br2) when heated with excess sodamide followed by treatment with dilute HCl gives [Q]. On warming [Q] with mercuric sulphate and dilute sulphuric acid yields [R] which gives positive Iodoform test but negative Tollens' test. The compound [P] is :
Identify A in the following reaction. [figure]
[figure] 'P' is
Choose the correct set of reagents for the following conversion. [figure]
Given below are two statements: In the light of the above statements, choose the correct answer from the options given below
Identify the structure of the final product (D) in the following sequence of the reactions : [figure] Total number of sp2 hybridised carbon atoms in product D is .
Predict the major product of the following reaction sequence: [figure]
Consider the following molecule(X). [figure] The major product formed when the given molecule (X) is treated with HBr (1 eq) is :
Which compound would give 3-methyl-6-oxoheptanal upon ozonolysis?
An optically active alkyl halide C4H9Br [A] reacts with hot KOH dissolved in ethanol and forms alkene [B] as major product which reacts with bromine to give dibromide [C]. The compound [C] is converted into a gas [D] upon reacting with alcoholic NaNH2. During hydration 18 gram of water is added to 1 mole of gas [D] on warming with mercuric sulphate and dilute acid at 333 K to form compound [E]. The IUPAC name of compound [E] is :
Given below are two statements: In the light of the above statements, choose the most appropriate answer from the options given below:
A molecule (P) on treatment with acid undergoes rearrangement and gives (Q). (Q) on ozonolysis followed by reflux under alkaline condition gives (R). The structure of (R) is given below. [figure] The structure of (P) is