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An alkene 'A' (molecular formula C(5)H(1...

An alkene 'A' (molecular formula `C_(5)H_(10)`) on ozonolysis gives a mixture of two compounds 'B' and 'C'. Compound 'B' gives positive Fehling's test and also forms iodoform on treatement with `I_(2)" and "NaOH`. Compound 'C' does not give Fehling's test but forms iodoform. Identify the compounds A, B and C. Write the reaction for ozonolysis and formation of iodoform from B and C.

Text Solution

AI Generated Solution

To solve the problem, we need to identify the alkene (A) with the molecular formula C5H10, and the two compounds (B and C) formed after ozonolysis. ### Step 1: Identify the Alkene (A) The molecular formula C5H10 indicates that the compound is an alkene. The degree of unsaturation can be calculated using the formula: \[ \text{Degree of Unsaturation} = \frac{C + 1 - H}{2} = \frac{5 + 1 - 10}{2} = \frac{-4}{2} = 1 \] This means there is one double bond in the structure. A possible structure for alkene A is 2-pentene (CH3-CH=CH-CH2-CH3). ...
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An alkene 'A' (Mol. formula C_5H_10 ) on ozonolysis gives a mixture of two compounds 'B' and 'C'. Compound 'B' gives positive Fehling's test and also forms iodoform on treatment with I_2 and NaOH. Compound 'C' does not give Fehling's test but forms iodoform. Identify the compounds A, B and C. Write the reaction for ozonolysis and formation of iodoform from Band C.

An alkene 'A' (Mol. formula C_5H_10 ) on ozonolysis gives a mixture of two compounds 'B' and 'C'. Compound 'B' gives positive Fehling's test and also forms iodoform on treatment with I_2 and NaOH. Compound 'C' does not give Fehling's test but forms iodoform. Identify the compounds A, B and C. Write the reaction for ozonolysis and formation of iodoform from Band C.

Knowledge Check

  • An alkene 'X' (molecular formula C_(5)H_(10) ) on ozonolysis gives a mixture of two compounds 'Y' and 'Z'. Compound 'Y' gives positive Fehling's test and also forms iodoform on treatement with I_(2)" and "NaOH . Compound 'Z' does not give Fehling's test but forms iodoform. Identify the compounds X, Y and Z. Write the reaction for ozonolysis and formation of iodoform from Y and Z.

    A
    `{:(" X"," Y"," Z"),(C_(6)H_(5)COCH_(3),CH_(3)CHO,CH_(3)COCH_(3)):}`
    B
    `{:(" X"," Y"," Z"),(CH_(3)-CH=underset(CH_(3))underset(|)C-CH_(3),CH_(3)CHO,CH_(3)COCH_(3)):}`
    C
    `{:(" X"," Y"," Z"),(CH_(3)CH_(2)CH=CH_(2),CH_(3)CH_(2)CHO,HCHO):}`
    D
    `{:(" X"," Y"," Z"),(CH_(3)-CH=CH-CH_(3),CH_(3)CHO,CH_(3)CHO):}`

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    An alkene 'A' (Mol. formula C_5H_10 ) on ozonolysis gives a mixture of two compounds 'B' and 'C'. Compound 'B' gives positive Fehling's test and also forms iodoform on treatment with I_2 and NaOH. Compound 'C' does not give Fehling's test but forms iodoform. Identify the compounds A, B and C. Write the reaction for ozonolysis and formation of iodoform from Band C.

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    Alkene (X) (C_(5)H_(10)) on ozonolysis gives a mixture of two compounds (Y) and (Z). Compound (Y) gives positive Fehling's test and iodoform test. Compound (Z) does not give Fehling's test but give iodoform test. Name the compound formed when Z reacts with Mg - Hg / H_(2)O

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