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A tertiary alcohol (H) upon acid-catalysed dehydration gives a product (I). Ozonolysis of (I) leads to compounds (J) and (K). Compound (J) upon reaction with KOH gives benzyl alcohol and a compound (L), whereas (K) on reaction with KOH gives only (M).
image
The structures of compounds (J), (K), and (L), respectively, are:
A. `Ph-overset(O)overset(|)(C)-CH_(3),Ph-CH_(2)-overset(O)overset(||)(C)-CH_(3)and Ph-CH_(2)-overset(O)overset(||)(C)-O^(Ө)K^(oplus)`
B. `Ph-overset(O)overset(||)(C)-H,Ph-CH_(2)-overset(O)overset(||)(C)-Hand Ph-overset(O)overset(||)(C)-O^(Ө)K^(oplus)`
C. `Ph-overset(O)overset(||)(C)-CH_(3),Ph-CH_(2)-overset(O)overset(||)(C)-Hand CH_(3)-overset(O)overset(||)(C)-O^(Ө)K^(oplus`
D. `Ph-overset(O)overset(||)(C)-H,Ph-overset(O)overset(||)(C)-CH_(3)and Ph-overset(O)overset(||)(C)-O^(Ө)K^(oplus`

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