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t-butyl alcohol reacts less rapidly with...

t-butyl alcohol reacts less rapidly with metalic sodium than the primary alcohol. Explain why?

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The `+I.E.` of three methyl groups on central C-atom of tert-butyl alcohol makes is partially negative with the result that it pushes the electron pair of `-OH` bond towards H-atom and thus H-atom is not replaced easily.
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BANSAL-ALCOHOL, ETHERS & PHENOL, OXIDATION & REDUCTION -Exercise 3
  1. What are the order of rates of oxidation with HIO(4) of the following ...

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  2. Complete the following equations (i) n-C(3)H(7)-CO(2)Hton-C(4)H(9)OH...

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  3. t-butyl alcohol reacts less rapidly with metalic sodium than the prima...

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  4. Ethyl alcohol reacts with HI but not with HCN. Explain why?

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  5. Write the structure of the principal organic product formed in the rea...

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  6. Complete the following series of equations by writing structural formu...

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  7. Predict the principal organic product of each of the following reactio...

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  8. Deduce the identify of the missinig compounds in the following raction...

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  9. Explain why ArOR ethers are cleaved to give RI and ArOH rather than Ar...

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  10. C(2)H(5)OHoverset(PCl(5))rarr(A)overset(KCN)rarr(B)overset(H(3)O^(+))r...

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  11. CH(3)CH(2)CH(2)OHoverset(PBr(5))rarr(A)overset(KOH(Alc))rarr(B)overset...

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  12. A compound (X) with the molecular formula C(3)H(8)O can be oxidized to...

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  13. Outline a mechanism to account for different isomer formed when react...

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  14. Differentiate: (a). 1-Hexanol and 1-chlorohexane (b). Diethyl ethe...

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  15. Complete the following equations & comment (i). MeOEtoverset(HI)to? ...

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  16. Diethyl ether behaves as base. Why?

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  17. Sometimes explosionn occurs durring the distilliation of an ether Expl...

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  18. Explain why ArOR ethers are cleaved to give RI and ArOH rather than Ar...

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  19. Complete the following with appropriate reagent:

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  20. Indicate steps which would convent: (A) Phenol to acetophenone (B)...

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