The graph provided is a plot of \( \log K \) versus \( \frac{1}{T} \), which is typically used to study the Arrhenius equation. According to the Arrhenius equation:
\[
K = A \exp\left(-\frac{E_a}{RT}\right)
\]
Taking the natural logarithm of both sides, we get:
\[
\log K = \log A - \frac{E_a}{2.303 R} \cdot \frac{1}{T}
\]
This equation represents a straight line, where the slope is \( -\frac{E_a}{2.303 R} \).
From the graph:
- The steepest slope corresponds to the highest activation energy \( E_{a1} \), as the slope is proportional to \( -E_a \).
- The second steepest slope corresponds to \( E_{a2} \), and
- The least steep slope corresponds to \( E_{a3} \).
Therefore, based on the graph:
\[
E_{a1}>E_{a2}>E_{a3}
\]
Thus, the correct order of activation energies is \( E_{a1}>E_{a2}>E_{a3} \).
Therefore, the correct answer is (1) \( E_{a1}>E_{a2}>E_{a3} \).