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प्रश्न
Complete the following reaction.
उत्तर
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संबंधित प्रश्न
Carbolic acid is ____________.
One mole of an organic compound (A) with the formula C3H8O reacts completely with two moles of HI to form X and Y. When Y is boiled with aqueous alkali it forms Z. Z answers the iodoform test. The compound (A) is ___________.
Is it possible to oxidise t-butyl alcohol using acidified dichromate to form a carbonyl compound?
0.44 g of a monohydric alcohol, when added to methyl magnesium iodide in ether, liberates at STP 112 cm3 of methane with PCC the same alcohol form a carbonyl compound that answers the silver mirror test. Identify the compound.
\[\begin{array}{cc}\phantom{..........}\ce{CH3}\\\phantom{.......}/\\\ce{C6H4}\\
\phantom{.......}\backslash\\\phantom{.........}\ce{OH}\end{array}\] is a/an ______.
What will be the product (X and A) for the following reaction:
\[\ce{acetylchloride ->[i) CH3MgBr][ii) H3O+]X->[acid K2Cr2O7]A}\]
Predict the major product, when 2-methyl but -2-ene is converted into an alcohol in the following method.
Acid catalysed hydration
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Draw the major product formed when 1-ethoxyprop-1-ene is heated with one equivalent of HI.
The correct IUPAC name of the compound,
\[\begin{array}{cc}
\ce{CH3}\phantom{......}\\
|\phantom{........}\\
\ce{H3C - CH - CH - CH - CH2 - OH}\\
|\phantom{............}|\phantom{........}\\
\ce{Cl}\phantom{...........}\ce{CH3}\phantom{......}
\end{array}\]
