The Wurtz reaction involves the coupling of alkyl halides in the presence of sodium metal to form higher alkanes. When ethyl iodide (C$_2$H$_5$I) and n-propyl iodide (C$_3$H$_7$I) are subjected to the Wurtz reaction, they can couple to form different hydrocarbons.
Step 1: The reaction between two ethyl iodide molecules can form butane (C$_4$H$_{10}$), as shown by: \[ C_2H_5I + C_2H_5I \xrightarrow{{Na}} C_4H_{10}. \] The reaction between ethyl iodide and n-propyl iodide can form pentane (C$_5$H$_{12}$), as shown by: \[ C_2H_5I + C_3H_7I \xrightarrow{{Na}} C_5H_{12}. \]
Step 2: However, propane (C$_3$H$_8$) cannot be formed in this reaction. This is because propane would require the coupling of two propyl iodide molecules, which is not possible here, as only ethyl and n-propyl iodides are involved.
Step 3: Thus, the hydrocarbon that will not be formed is propane.
The speed at which a chemical reaction takes place is called the rate of reaction. The rate of reaction depends on various factors like concentration of the reactants, temperature, etc. The relation between the rate of reaction and the concentration of reacting species is represented by the equation \( r = k[A]^x[B]^y \), where \( x \) and \( y \) are the order of the reaction with respect to the reactants A and B, respectively. The overall order of the reaction is \( x + y \). The rate of reaction can also be increased by the use of a catalyst which provides an alternate pathway of lower activation energy. It increases the rate of forward and backward reactions to an equal extent. It does not alter the Gibbs energy of the reaction.
Which of the following are ambident nucleophiles?
[A.] CN$^{\,-}$
[B.] CH$_{3}$COO$^{\,-}$
[C.] NO$_{2}^{\,-}$
[D.] CH$_{3}$O$^{\,-}$
[E.] NH$_{3}$
Identify the anomers from the following.

The standard Gibbs free energy change \( \Delta G^\circ \) of a cell reaction is \(-301 { kJ/mol}\). What is \( E^\circ \) in volts?
(Given: \( F = 96500 { C/mol}\), \( n = 2 \))