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ChemistryHardMCQ2020 · 03 Sep Shift 2

Q42.The compound A in the following reactions is: (i) CH3 MgBr /H2O (i) O3 −−A → B → C + D (ii) Conc. H2 SO4 /Δ (ii) Zn /H2O (1) (2) (3) (4)

What This Question Tests

This complex multi-step synthesis problem requires working backward from the final products (C and D) through ozonolysis, then determining the alkene (B), and finally identifying the starting alcohol (A) from its Grignard reaction product.

Concepts Tested

Grignard reagent reaction with ketonesOzonolysis of alkenesDehydration of alcoholsSynthesis of organic compounds

📚 NCERT Sections This Tests

7.21Name The Reagents Used In The Following Reactions:

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7.21 Name the reagents used in the following reactions: (i) Oxidation of a primary alcohol to carboxylic acid. (ii) Oxidation of a primary alcohol to aldehyde. (iii) Bromination of phenol to 2,4,6-tribromophenol. (iv) Benzyl alcohol to benzoic acid. (v) Dehydration of propan-2-ol to propene. (vi) Butan-2-one to butan-2-ol.

8.17Complete Each Synthesis By Giving Missing Starting Material, Reagent Or Products

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8.17 Complete each synthesis by giving missing starting material, reagent or products

7.20How Are The Following Conversions Carried Out?

Chemistry Class 12 · Chapter 7

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7.20 How are the following conversions carried out? (i) Propene ® Propan-2-ol. (ii) Benzyl chloride ® Benzyl alcohol. (iii) Ethyl magnesium chloride ® Propan-1-ol. (iv) Methyl magnesium bromide ® 2-Methylpropan-2-ol.