- AAt a slower rate
- BAt a faster rate
- CWith equal rate
- DWith equal rate (or) different rate depending upon the temperature.
Explanation:
Bromination of an alkane occurs at a slower rate than chlorination of an alkane.
As we know that halogenation involves the formation of a carbon-halogen bond. Now, the ease of halogenation will certainly depend on the carbon-halogen bond strength.
Bond formation energy of C−Cl is higher than that of C−Br bond.
So, the ease of bromination is lower than the ease of chlorination.
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Propene $\xrightarrow{{C{l_2}/500\,{}^oC}}A\xrightarrow[{{\text{dryether}}}]{{Na}}B$
$B$ is
$I$. Valence bond theory cannot explain the color exhibited by transition metal complexes
$II$. Valence bond theory can predict quantitatively the magnetic properties of transition metal complexes
$III$. Valence bond theory cannot distinguish ligands as weak and strong field ones
$M + L \rightleftharpoons ML$
$ML + L \rightleftharpoons M{L_2}$
are $4$ and $3$. Hence, overall stability constant for
$M + 2L \rightleftharpoons M{L_2}$ is