To determine which drug will be the first to degrade by 50%, we need to understand the degradation kinetics of zero-order, first-order, and second-order reactions and how these relate to the time required for a substance to reduce by 50% (half-life).
- Zero-order kinetics (Drug A): The rate of degradation is constant and does not depend on the concentration of the drug. The formula for zero-order reactions is: \([\text{A}] = [\text{A}_0] - kt\), where \([\text{A}]\) is the concentration at time \(t\), \([\text{A}_0]\) is the initial concentration, \(k\) is the rate constant. The time to degrade by 50% is: \(t_{50\%} = \frac{[\text{A}_0]}{2k}\).
- First-order kinetics (Drug B): The rate of degradation is directly proportional to the concentration of the drug. The formula is: \([\text{A}] = [\text{A}_0]e^{-kt}\). The time to degrade by 50% (half-life) is independent of the initial concentration: \(t_{50\%} = \frac{\ln(2)}{k}\).
- Second-order kinetics (Drug C): The rate depends on the square of the concentration of the drug. The formula is: \(\frac{1}{[\text{A}]} = \frac{1}{[\text{A}_0]} + kt\). The time to degrade by 50% is: \(t_{50\%} = \frac{1}{k[\text{A}_0]}\).
Given that all drugs have the same rate constant \((k)\), we can compare the times for the concentration of each drug to reduce by 50%:
- For Drug A (zero-order), the time depends on the initial concentration.
- For Drug B (first-order), the half-time is a constant value \(t_{50\%} = \frac{\ln(2)}{k}\).
- For Drug C (second-order), the time to degrade by 50% is inversely proportional to the initial concentration. If the concentration is high, this can be very quick.
From the formulas, \(t_{50\%}\)for second-order (Drug C) is smallest compared to the zero-order and first-order when given the same initial concentration and rate constant.
Thus, the correct statement is: Drug ‘C’ will be the first to degrade by 50%.