Question
(i) How will you prepare methanol from formaldehyde without using a reducing agent?
(ii) Why is Rochelle salt used in Fehling's solution?

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Write the reagents used in the following reactions:
  1. $\text{C}_{6}\text{H}_{5}-\text{CO}-\text{CH}_{3}\xrightarrow{\text{ }\ \ \ \ \ \ {?}\ \\ \ \ \ \ \ }\text{C}_{6}\text{H}_{5}-\text{CH}_{2}-\text{CH}_{3}$
  2. $\text{CH}_{3}-\text{COOH}\xrightarrow{\text{ }\ \ \ \ \ \ {?}\ \\ \ \ \ \ \ }\text{CH}_{3}-\text{COCl}$
Compare the chemistry of the actinoid with that of lanthanoids with reference to: Electronic configuration:
What happens when
i. a pressure greater than osmotic pressure is applied on the solution side separated from solvent by a semipermeable membrane?
ii. acetone is added to pure ethanol?
An organic compound ‘$X$’ having molecular formula $\ce{C_4H_8O}$ gives orange $-$ red ppt. with $2, 4-\ce{DNP}$ reagent. It does not reduce Tollens’ reagent but gives yellow ppt. of iodoform on heating with $\ce{NaOI}$. Compound $X$ on reduction with $\ce{LiAlH_4}$ gives compound ‘$Y$’ which undergoes dehydration reaction on heating with conc. $\ce{H_2SO_4}$ to form But $-2$-ene. Identify the compounds $X$ and $Y$.
a. On the basis of crystal field theory, write the electronic configuration for $d ^4$ with a strong field ligand for which $\Delta_0>P$.
b. A solution of $\left[ Ni \left( H _2 O \right)_6\right]^{2+}$ is green but a solution of $\left[ Ni ( CO )_4\right]$ is colourless. Explain.
[Atomic number : $Ni =28$ ]
Write structures of different dihalogen derivatives of propane.
Write note on physical properties of Ianthanoids.
Give reasons for the following observations:
Haloarenes are less reactive than haloalkanes towards nucleophillic substitution reaction.
Answer the following:
(a) A reaction is 50% complete in 2 hours and 75% complete in 4 hours. What is the order of the reaction?
(b) For which type of reactions, order and molecularity have the same value?
How are interhalogen compounds formed? What general compositions can be assigned to them?