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Two isomers A and B having molecular for...

Two isomers A and B having molecular formula `C_3H_8O` when passed separately over heated alumina produce compound C with molecular formula `C_3H_6`. C on ozonolysis produces D and E. Between them, D undergoes iodoform reaction but not E. Identify A, B, C, D and E. Write the equations of the reactions concerned.

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To solve the problem step by step, we need to identify the isomers A and B, the compound C formed from them, and the products D and E resulting from ozonolysis of C. ### Step 1: Identify Isomers A and B The molecular formula given is C₃H₈O. The possible isomers for this formula include: 1. **Isomer A**: Propanol (CH₃CH₂CH₂OH) - a straight-chain alcohol (1-propanol). 2. **Isomer B**: Isopropanol (CH₃CHOHCH₃) - a branched-chain alcohol (2-propanol). ### Step 2: Reaction with Heated Alumina ...
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ICSE-PROLEMS BASED ON CHEMICAL STRUCTURES AND REACTIONS -QUESTIONS
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  15. CH3 - overset(O)overset(||)C - OH overset(2RLi)toA , A overset(H3O^(+)...

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  16. Anorganic compound with molecular formula C9H10O forms 2,4-DNP derivat...

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  17. Compound A (C6H12O2) on reduction with LiAlH4, yielded two compounds B...

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  19. Anorganic compound (A) having molecular formula C9H10O forms an orang...

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