Given below are two statements:
Statement - I: Since Fluorine is more electronegative than nitrogen, the net dipole moment of $$\mathrm{NF}_3$$ is greater than $$\mathrm{NH}_3$$.
Statement - II: In $$\mathrm{NH}_3$$, the orbital dipole due to lone pair and the dipole moment of $$\mathrm{NH}$$ bonds are in opposite direction, but in $$\mathrm{NF}_3$$ the orbital dipole due to lone pair and dipole moments of N-F bonds are in same direction.
In the light of the above statements, choose the most appropriate from the options given below:
A and B formed in the following reactions are:
$$\begin{aligned} & \mathrm{CrO}_2 \mathrm{Cl}_2+4 \mathrm{NaOH} \rightarrow \mathrm{A}+2 \mathrm{NaCl}+2 \mathrm{H}_2 \mathrm{O}, \\ & \mathrm{A}+2 \mathrm{HCl}+2 \mathrm{H}_2 \mathrm{O}_2 \rightarrow \mathrm{B}+3 \mathrm{H}_2 \mathrm{O} \end{aligned}$$
Given below are two statements:
Statement - I: High concentration of strong nucleophilic reagent with secondary alkyl halides which do not have bulky substituents will follow $$\mathrm{S}_{\mathrm{N}}{ }^2$$ mechanism.
Statement - II: A secondary alkyl halide when treated with a large excess of ethanol follows $$\mathrm{S}_{\mathrm{N}}{ }^1$$ mechanism.
In the light of the above statements, choose the most appropriate from the options given below:
Choose the correct statements about the hydrides of group 15 elements.
A. The stability of the hydrides decreases in the order $$\mathrm{NH}_3>\mathrm{PH}_3>\mathrm{AsH}_3> \mathrm{SbH}_3>\mathrm{BiH}_3$$.
B. The reducing ability of the hydride increases in the order $$\mathrm{NH}_3<\mathrm{PH}_3<\mathrm{AsH}_3 <\mathrm{SbH}_3<\mathrm{BiH}_3$$.
C. Among the hydrides, $$\mathrm{NH}_3$$ is strong reducing agent while $$\mathrm{BiH}_3$$ is mild reducing agent.
D. The basicity of the hydrides increases in the order $$\mathrm{NH}_3<\mathrm{PH}_3<\mathrm{AsH}_3< \mathrm{SbH}_3<\mathrm{BiH}_3$$.
Choose the most appropriate from the options given below :
Given below are two statements: One is labelled as Assertion A and the other is labelled as Reason R:
Assertion A: $$\mathrm{H}_2 \mathrm{Te}$$ is more acidic than $$\mathrm{H}_2 \mathrm{~S}$$.
Reason R: Bond dissociation enthalpy of $$\mathrm{H}_2 \mathrm{Te}$$ is lower than $$\mathrm{H}_2 \mathrm{~S}$$.
In the light of the above statements, choose the most appropriate from the options given below:
Reduction potential of ions are given below:
$$\begin{array}{ccc} \mathrm{ClO}_4^{-} & \mathrm{IO}_4^{-} & \mathrm{BrO}_4^{-} \\ \mathrm{E}^{\circ}=1.19 \mathrm{~V} & \mathrm{E}^{\circ}=1.65 \mathrm{~V} & \mathrm{E}^{\circ}=1.74 \mathrm{~V} \end{array}$$
The correct order of their oxidising power is :
Given below are two statements:
Statement - I: Along the period, the chemical reactivity of the elements gradually increases from group 1 to group 18 .
Statement - II: The nature of oxides formed by group 1 elements is basic while that of group 17 elements is acidic.
In the light of the above statements, choose the most appropriate from the options given below:
The total number of correct statements, regarding the nucleic acids is _________.
A. RNA is regarded as the reserve of genetic information
B. DNA molecule self-duplicates during cell division
C. DNA synthesizes proteins in the cell
D. The message for the synthesis of particular proteins is present in DNA
E. Identical DNA strands are transferred to daughter cells.
$$\mathrm{NO}_2$$ required for a reaction is produced by decomposition of $$\mathrm{N}_2 \mathrm{O}_5$$ in $$\mathrm{CCl}_4$$ as by equation
$$2 \mathrm{~N}_2 \mathrm{O}_{5(\mathrm{~g})} \rightarrow 4 \mathrm{NO}_{2(\mathrm{~g})}+\mathrm{O}_{2(\mathrm{~g})}$$
The initial concentration of $$\mathrm{N}_2 \mathrm{O}_5$$ is $$3 \mathrm{~mol} \mathrm{~L}^{-1}$$ and it is $$2.75 \mathrm{~mol} \mathrm{~L}^{-1}$$ after 30 minutes.
The rate of formation of $$\mathrm{NO}_2$$ is $$\mathrm{x} \times 10^{-3} \mathrm{~mol} \mathrm{~L}^{-1} \mathrm{~min}^{-1}$$, value of $$\mathrm{x}$$ is _________. (nearest integer)
Number of complexes which show optical isomerism among the following is ________.
$$\text { cis- }\left[\mathrm{Cr}(\mathrm{ox})_2 \mathrm{Cl}_2\right]^{3-},\left[\mathrm{Co}(\text {en})_3\right]^{3+}, \text { cis- }\left[\mathrm{Pt}(\text {en})_2 \mathrm{Cl}_2\right]^{2+}, \text { cis- }\left[\mathrm{Co}(\text {en})_2 \mathrm{Cl}_2\right]^{+}, \text {trans- }\left[\mathrm{Pt}(\text {en})_2 \mathrm{Cl}_2\right]^{2+}, \text { trans- }\left[\mathrm{Cr}(\mathrm{ox})_2 \mathrm{Cl}_2\right]^{3-}$$
Two reactions are given below:
$$\begin{aligned} & 2 \mathrm{Fe}_{(\mathrm{s})}+\frac{3}{2} \mathrm{O}_{2(\mathrm{~g})} \rightarrow \mathrm{Fe}_2 \mathrm{O}_{3(\mathrm{~s})}, \Delta \mathrm{H}^{\circ}=-822 \mathrm{~kJ} / \mathrm{mol} \\ & \mathrm{C}_{(\mathrm{s})}+\frac{1}{2} \mathrm{O}_{2(\mathrm{~g})} \rightarrow \mathrm{CO}_{(\mathrm{g})}, \Delta \mathrm{H}^{\circ}=-110 \mathrm{~kJ} / \mathrm{mol} \end{aligned}$$
Then enthalpy change for following reaction $$3 \mathrm{C}_{(\mathrm{s})}+\mathrm{Fe}_2 \mathrm{O}_{3(\mathrm{~s})} \rightarrow 2 \mathrm{Fe}_{(\mathrm{s})}+3 \mathrm{CO}_{(\mathrm{g})}$$ is _______ $$\mathrm{kJ} / \mathrm{mol}$$.