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प्रश्न
Write the IUPAC name of the following compound.
\[\begin{array}{cc}
\phantom{.}\ce{CH3 - CH - CH - CH - CH - CH3}\phantom{}\\
\phantom{......}|\phantom{......}|\phantom{......}|\phantom{.....}|\phantom{........}\\
\phantom{...}\ce{CH3}\phantom{...}\ce{OH}\phantom{...}\ce{C2H5}\phantom{.}\ce{OH}\phantom{...}\end{array}\]
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उत्तर
3-Ethyl-5-methylhexane-2, 4-diol
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संबंधित प्रश्न
How do you convert the following:
Ethanol to Propan-2-ol
Write the mechanism of the following reaction :
\[\ce{C2H5OH->[H2SO4][443K]CH2=CH2 + H2O}\]
If ethanol dissolves in water, then which of the following would be observed:
Phenol is less acidic than ______.
Name the enzymes and write the reactions involved in the preparation of ethanol from sucrose by fermentation.
Match the items of column I with items of column II.
| Column I | Column II | |
| (i) | Antifreeze used in car engine | (a) Neutral ferric chloride |
| (ii) | Solvent used in perfumes | (b) Glycerol |
| (iii) | Starting material for picric acid | (c) Methanol |
| (iv) | Wood spirit | (d) Phenol |
| (v) | Reagent used for detection of phenolic group | (e) Ethleneglycol |
| (vi) | By product of soap industry used in cosmetics | (f) Ethanol |
Match the items of column I with items of column II.
| Column I | Column II | |
| (i) | Methanol | (a) Conversion of phenol to o-hydroxysalicylic acid |
| (ii) | Kolbe’s reaction | (b) Ethyl alcohol |
| (iii) | Williamson’s synthesis | (c) Conversion of phenol to salicylaldehyde |
| (iv) | Conversion of 2° alcohol to ketone | (d) Wood spirit |
| (v) | Reimer-Tiemann reaction | (e) Heated copper at 573 K |
| (vi) | Fermentation | (f) Reaction of alkyl halide with sodium alkoxide |
Convert the following:
Propanenitrile to ethanol.
Which reagent can convert acetic acid into ethanol?
Liquor poisoning is due to
If the starting material is 1-methyl-1,2-epoxy cyclopentane, of absolute configuration, decide which one compound correctly represents the product of its reaction with sodium methoxide in methanol.
How methanol is obtained from methanal.
3, 3-dimethyl-1-butene was subject to following reactions:

