An alkene ‘A' (Mol. formula C5H10) on ozonolysis gives a mixture of two compounds 'B' and 'C'. Compound 'B' gives positive Fehlings test and also forms iodoform on treatment with I2 and NaOH. Compound 'C' does not give Fehling’s test but forms iodoform. The compound 'C' is

Question

An alkene ‘A' (Mol. formula C5H10) on ozonolysis gives a mixture of two compounds 'B' and 'C'. Compound 'B' gives positive Fehlings test and also forms iodoform on treatment with I2 and NaOH. Compound 'C' does not give Fehling’s test but forms iodoform. The compound 'C' is (A) acetaldehyde (B) formic acid (C) benzaldehyde (D) acetone

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underset overset text2-Methylbut-2-ene(A)CH3 -CH = underset overset|CH3C - CH3 xrightarrow[(ii)Zn/H2O](i)O3 <img class="img-fluid question-image" alt="image" src="https://cdn.tardigrade.in/img/question/chemistry/b6d819238b600a619be229242c76057b-.png" />

Q. An alkene ‘A' (Mol. formula $C_{5} H_{10})$ on ozonolysis gives a mixture of two compounds 'B' and 'C'. Compound 'B' gives positive Fehlings test and also forms iodoform on treatment with $I_{2}$ and $N a O H$ . Compound 'C' does not give Fehling’s test but forms iodoform. The compound 'C' is

acetaldehyde

formic acid

benzaldehyde

acetone

$(A) 2-Methylbut-2-ene C H_{3} - C H = C H_{3} ∣ C - C H_{3} (i) O_{3} (ii) Z n / H_{2} O$

Q. An alkene ‘A' (Mol. formula C5​H10​) on ozonolysis gives a mixture of two compounds 'B' and 'C'. Compound 'B' gives positive Fehlings test and also forms iodoform on treatment with I2​ and NaOH. Compound 'C' does not give Fehling’s test but forms iodoform. The compound 'C' is

acetaldehyde

formic acid

benzaldehyde

acetone

(A)2-Methylbut-2-ene​CH3​−CH=CH3​∣​C​−CH3​​(i)O3​(ii)Zn/H2​O​

$(A) 2-Methylbut-2-ene C H_{3} - C H = C H_{3} ∣ C - C H_{3} (i) O_{3} (ii) Z n / H_{2} O$