



To understand the graphical representation of a first-order reaction, we need to consider the kinetics of such reactions. In a first-order reaction, the rate of reaction depends linearly on the concentration of one reactant.
The rate equation for a first-order reaction can be expressed as:
\[-\frac{d[A]}{dt} = k[A]\]Where:
Integrating this equation, we get the expression:
\[\ln [A] = \ln [A_0] - kt\]Where:
This equation can be rearranged into the linear form of a straight line:
\[\ln [A] = -kt + \ln [A_0]\]Comparing it to the standard line equation \( y = mx + c \), where \( y = \ln [A] \), \( m = -k \), \( x = t \), and \( c = \ln [A_0] \), we see that a plot of \( \ln [A] \) versus \( t \) should give a straight line with a slope equal to \( -k \).
Therefore, the graphical representation of a first-order reaction should depict a straight line when plotting the natural logarithm of concentration against time.
Now, examining the given options, the graph that correctly represents a first-order reaction is:

This graph shows a linear decrease in \( \ln [A] \) versus time (\( t \)), which is characteristic of a first-order reaction.
| Molisch's lest | Barfoed Test | Biuret Test | |
|---|---|---|---|
| A | Positive | Negative | Negativde |
| B | Positive | Positive | Negative |
| C | Negative | Negative | Positive |