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Compounds P(C6H10) does not have any geo...

Compounds P`(C_6H_10)` does not have any geometrical isomer.On ozonolysis, two products `R(C_3H_4O)` and `Q(C_3H_6O)` are formed.R gives negative iodoform test while Q responds positively towards `I_2//NaOH` solution.S, another isomer of P is an unsymetrical alkene and on ozonolysis produces `T(C_6H_(10_7))` which also gives a yellow precipitate with `l_2//NaOH` solution and also positive test with Tollen's reagent Which of the following does not represent any of the molecules amongst P,Q,R,S & T.

A

B

C

D

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The correct Answer is:
To solve the problem, we need to analyze the given compounds and their properties step-by-step. ### Step 1: Analyze Compound P (C₆H₁₀) - Compound P does not have any geometrical isomers, which suggests it has a symmetrical structure. - A possible structure for P could be 2,3-dimethyl-2-butene, which has no geometrical isomers. ### Step 2: Ozonolysis of Compound P - Upon ozonolysis, P yields two products: R (C₃H₄O) and Q (C₃H₆O). - R gives a negative iodoform test, indicating it does not have a methyl ketone group (–C(=O)CH₃). - Q gives a positive iodoform test, indicating it has a methyl ketone group. ### Step 3: Identify Structures of R and Q - Since R does not give a positive iodoform test, it could be an aldehyde or an alcohol. A possible structure for R is propanal (CH₃CH₂CHO). - For Q, since it gives a positive iodoform test, it could be a methyl ketone. A possible structure for Q is 2-butanone (CH₃C(=O)CH₂CH₃). ### Step 4: Analyze Compound S - S is another isomer of P and is an unsymmetrical alkene. - Upon ozonolysis, S produces T (C₆H₈O), which gives a yellow precipitate with I₂/NaOH (indicating a positive iodoform test) and a positive test with Tollens' reagent (indicating an aldehyde). ### Step 5: Identify Structure of T - Since T gives a yellow precipitate with I₂/NaOH, it must contain a methyl ketone group. - A possible structure for T could be 3-hexanone, which can also yield an aldehyde upon ozonolysis. ### Step 6: Evaluate Given Options - We need to identify which of the given compounds does not correspond to any of the structures P, Q, R, S, or T. - If we analyze the molecular formulas and the properties of the compounds, we can conclude that: - Compound A (C₃H₄O) could be R. - Compound B (C₆H₈O₂) does not fit any of the identified compounds. - Compound C (C₆H₁₀O) could be T. - Compound D (C₃H₆O) could be Q. ### Conclusion - The compound that does not represent any of the molecules among P, Q, R, S, and T is **Compound B (C₆H₈O₂)**.

To solve the problem, we need to analyze the given compounds and their properties step-by-step. ### Step 1: Analyze Compound P (C₆H₁₀) - Compound P does not have any geometrical isomers, which suggests it has a symmetrical structure. - A possible structure for P could be 2,3-dimethyl-2-butene, which has no geometrical isomers. ### Step 2: Ozonolysis of Compound P - Upon ozonolysis, P yields two products: R (C₃H₄O) and Q (C₃H₆O). ...
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