Match the following:
Column-$1$ (Reaction)Column-$2$ (Main product)
$A$. $4FeCl_3 + 3K_4[Fe(CN)_6] \rightarrow$$I$. $Fe_4[Fe(CN)_6]_3$
$B$. $ZnCl_2 + 4NaOH \rightarrow$$V$. $Na_2ZnO_2$
$C$. $2FeCl_3 + H_2S \rightarrow$$II$. $FeCl_2$

  • A
    $A$$B$$C$
    $I$$III$$VI$
  • B
    $A$$B$$C$
    $I$$V$$II$
  • C
    $A$$B$$C$
    $IV$$V$$II$
  • D
    $A$$B$$C$
    $IV$$III$$VI$

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Similar Questions

Among the statements $(a)-(d)$,the incorrect ones are:
$(a)$ Octahedral $Co(III)$ complexes with strong field ligands have very high magnetic moments.
$(b)$ When $\Delta_{0} < P$,the $d-$electron configuration of $Co(III)$ in an octahedral complex is $t_{2g}^{4} e_{g}^{2}$.
$(c)$ Wavelength of light absorbed by $[Co(en)_{3}]^{3+}$ is lower than that of $[CoF_{6}]^{3-}$.
$(d)$ If the $\Delta_{0}$ for an octahedral complex of $Co(III)$ is $18,000 \ cm^{-1}$,the $\Delta_{t}$ for its tetrahedral complex with the same ligand will be $16,000 \ cm^{-1}$.

The given complex $M(ABCDEF)$ exhibits which of the following isomerism?

The correct statements from the following are:
$A$. The strength of anionic ligands can be explained by crystal field theory.
$B$. Valence bond theory does not give a quantitative interpretation of kinetic stability of coordination compounds.
$C$. The hybridization involved in the formation of $\left[Ni(CN)_4\right]^{2-}$ complex is $dsp^2$.
$D$. The number of possible isomer$(s)$ of $cis-\left[PtCl_2(en)_2\right]^{2+}$ is one.
Choose the correct answer from the options given below:

The configurations for the complex $[Co(en)(NH_3)_2Br_2]^+$ are shown. Which of the following statements is incorrect?

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The correct option(s) about entropy $(S)$ is(are)
$[R =$ gas constant, $F =$ Faraday constant, $T =$ Temperature $]$
$(A)$ For the reaction, $M_{(s)} + 2H^{+}_{(aq)} \rightarrow H_{2(g)} + M^{2+}_{(aq)}$, if $\frac{dE_{cell}}{dT} = \frac{R}{F}$, then the entropy change of the reaction is $R$ (assume that entropy and internal energy changes in entropy and internal energy are temperature independent).
$(B)$ The cell reaction, $Pt_{(s)} \mid H_2(g, 1 \ bar) \mid H^{+}(aq, 0.01 \ M) \parallel H^{+}(aq, 0.1 \ M) \mid H_2(g, 1 \ bar) \mid Pt_{(s)}$, is an entropy driven process.
$(C)$ For racemization of an optically active compound, $\Delta S > 0$.
$(D)$ $\Delta S > 0$, for $[Ni(H_2O)_6]^{2+} + 3en \rightarrow [Ni(en)_3]^{2+} + 6H_2O$ (where $en =$ ethylenediamine).

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