The Collision theory states that every reaction proceeds by the collision in between the reactant molecules. However, to bring about a chemical reaction, the reactants must collide with a certain minimum amount of energy. Such collisions that make the reactions happen are called effective collisions.
Definition: Collision Theory states that only those reactant molecules colliding with the threshold energy may lead to the product formation. |
Collision Theory Chemistry Questions with Solutions
Q1: Why is the instantaneous rate of reaction preferred over the average rate? Or why is the rate of the reaction not uniform throughout?
Answer: This is because the rate of any reaction depends upon the reactantβs concentration at the given time. As the concentration of each reactant decreases with time, the rate of reaction also keeps changing.
Q2. Can a reaction have zero activation energy (Ea)?
Answer: According to the Arrhenius equation: k = A.e-Ea/RT
If Ea = 0, then, k = A.e0 = A
This means that the rate constant is equal to the collision frequency and hence every collision leads to a chemical reaction which is not true. Hence, Ea cannot be zero.
Q3. A first order reaction takes 69.3 minutes to reach 50% of its completion. Determine the time required for 80% completion of the reaction.
Answer: From 1st order reaction we have: k = 0.693 / t1/2
As t1/2 = 69.3 min, k = 0.693 / 69.3 min-1 = 0.01 min-1
Hence, k = 0.01 min-1 for the reaction
Now,
Given: x = 80% of a = 0.8a
Hence,
Q4. From the given expressions, determine the order of the reactions and the dimension of rate constants.
- C2H5Cl (g) β C2H4 (g) + HCl (g); Rate = k[C2H5Cl]
- 3NO (g) β N2O (g) + NO2 (g); Rate = k[NO]2
Answer: The order of the reaction and dimension of rate constant are hereunder.
- From the rate law expression, order of the reaction = 1
Similarly, dimensions of k can be calculated from the rate law as:
k = Rate / [C2H5Cl] = mol L-1 s-1 / mol L-1 = s-1
Hence, the dimension of k is s-1.
- From the rate law expression, order of the reaction = 2
Similarly, dimensions of k can be calculated from the rate law as:
k = Rate / [NO]2 = mol L-1 s-1 / (mol L-1)2 = L mol-1 s-1
Hence, the dimension of k is L mol-1 s-1.
Q5. Will the value of rate constant be feasible at extremely high temperature i.e. t = β?
Answer: At t = β, k = A.e-Ea/RT = A.e-Ea/Rβ = A.e0 = A
This implies that at t = β, the rate constant is equal to the frequency of collisions. However, this is not true as all the collisions may not lead the reactants into products.
Q6. Calculate the half-life period of a first order reaction given the rate constant of the reaction is 200 s-1.
Answer: The half-life period of a first order reaction is given by:
t1/2 = 0.693/k
Hence, t1/2 = 0.693 / 200 s-1 = 0.346 x 10-2 s = 3.46 x 10-3 s
Q7. An archaeological artifact found in a wooden piece was left with only 80% 14C. Estimate the age of the sample.
Answer: The half-life period for the radioactive decay of 14C is 5730 years. The Radioactive decay follows the first order kinetics.
Hence, the Decay constant (k) = 0.693 / t1/2 = 0.693 / 5730 yr
Hence, the age of the sample can be calculated as:
Hence, the age of the sample is 1845 years.
Q8. In the rate expression, the term (-dx/dt) refers to
- Instantaneous rate of the reaction
- Concentration of reactants
- Average rate of reaction
- Increase in the concentration of reactants
Answer: (a.)
Explanation: The Instantaneous rate of the reaction is calculated for a very small value of concentration of reactants/ products in infinitesimally time period
Q9. The threshold energy is equal to
- Average kinetic energy of molecules of reactants
- Normal energy of reactants – activation energy
- Activation energy + normal energy of reactants
- Activation energy – normal energy of reactants
Answer: (c.)
Explanation: The activation energy is the excess energy that is acquired by the molecules in order to achieve the threshold energy.
Q10. The influence of temperature on the rate of the reaction is determined by
- Arrhenius equation
- Nernstβs equation
- Gibbs-Helmholtz equation
- Vanβt Hoff equation
Answer: (a.)
Explanation: The Arrhenius equation has a direct relation between temperature and the rate constant.
Q11. Which plot can give the value of activation energy?
- C versus T
- 1/k versus T
- Log k versus 1/T
- k versus T
Answer: (c.)
Explanation: The slope of the log k versus 1/T curve gives the value of activation energy.
Slope = Ea / 2.303R
Q12. The number of molecules colliding per unit volume per second of the reaction mixture is known as _____.
Answer: Collision Frequency
Q13. Give one example when the molecularity and the order of the reaction are the same.
Answer: The example is:
CH3COOC2H5 + NaOH β CH3COONa + C2H5OH
In this reaction, molecularity = order= 2
Q14. Verify the statement: Slow reactions require less energy of activation as compared to the fast reactions.
Answer: This statement is wrong as the energy of activation is inversely proportional to the rate of the reaction.
Q15. The experimentally determined rate expression for the reaction: NO2(g) + CO(g) β CO2(g) + NO(g) is Rate = k[NO2]2. Suggest the mechanism for the reaction.
Answer: As the rate depends upon the decomposition of NO2,the possible mechanism can be:
Step 1: NO2 + NO2 β NO + NO3 (slow)
Step 2: NO3 + CO β CO2 + NO2 (fast)
Practise Questions on Carbonyl Compounds
Q1. Consider the following one-step reaction:
2(NO) (g) + O2 (g) β 2NO2 (g)
If the volume of the vessel is lowered to β of its original volume, what will be the effect on the rate of the reaction?
Q2. Why are the reactions of higher order less in number?
Q3. Calculate the rate for the given reaction during the period when [A] decreases from 0.5 mol/L to 0.4 mol/L in 10 min.
2A β Products
Q4. The rate expression for the reaction CH3OCH3 β CH4 + H2 + CO is given as:
Taking pressure in bar and time in minutes, calculate the units of the rate and the rate constant.
Q5. A reaction is first order in terms of A and zeroth order in terms of B. Fill in the blanks for the reaction in between A and B.
Experiment | [A]: mol L-1 | [B]: mol L-1 | Initial Rate: mol L-1 min-1 |
---|---|---|---|
I | 0.1 | 0.1 | 2.0 x 10-2 |
II | __ | 0.2 | 4.0 x 10-2 |
III | 0.4 | 0.4 | __ |
IV | __ | 0.2 | 2.0 x 10-2 |
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