Which of the following compounds is most prone to oxidation?
1. | \(\mathrm{CH}_3-\mathrm{CHOH}-\mathrm{CH}_3\) |
2. | ![]() |
3. | \(\mathrm{CH}_3-\mathrm{CH}_2-\mathrm{O}-\mathrm{CH}_2-\mathrm{CH}_3\) |
4. | ![]() |
Which of the following react with HBr at faster rate?
1. | \(\mathrm{NaBH}_4 \) | 2. | \(\mathrm{LiAlH}_4 \) |
3. | \(PCC \) | 4. | \(\mathrm{KMnO}_4\) |
1. | 2. | ||
3. | |
4. | |
(A) Product (A) is:
(a) No reaction
(b)
(c)
(d)
Consider the following alcohols,
(I) (II)
(III) (IV)
The order of decreasing reactivities of these alcohols towards nucleophilic substitution with HBr is:-
(a) III>I>IV>II
(b) III>I>II>IV
(c) I>III>IV>II
(d) I>III>II>IV
; Chemist added extra 0.5 mole of Et-Li in above reaction to obtain product (A), which is ?
Which is the best reagent to convert isopropyl alcohol to isopropyl bromide ?
(1) HBr
(2) SOBr2
(3) Br2
(4) CH3MgBr
Find missing reagents.
1. x = LiAlH4, y = NaBH4
2. x = LiAIH4 / AlCl3, y = LiAlH4
3. x = LiAIH4, Y = LiAIH4 / AlCl3
4. x = H2 / Ni, y = H2 / Pt