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Collision theory is satisfactory for: (a) First order reactions (b) Zero order reactions (c) Bimolecular reactions (d) Any order reactions

Short Answer

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Collision theory is satisfactorily applicable to (a) First order reactions and (c) Bimolecular reactions.

Step by step solution

01

Understanding Collision Theory

Collision theory states that for a reaction to occur, it's necessary for reactant particles to collide with sufficient energy and proper orientation. The theory applies best to reactions involving gases and liquids where collisions are frequent.
02

Applying Collision Theory to Reaction Orders

First-order reactions depend on the frequency of collisions of one reactant. Bimolecular reactions, or second-order reactions, involve the collision between two reactant molecules. Collision theory explains these types of reactions effectively as it is based on the collisions of molecules.
03

Evaluating Collision Theory for Zero Order Reactions

Zero-order reactions have a rate that is independent of the concentration of reactants. These reactions often occur on surfaces and their rate is determined by the availability of active sites. Collision theory is not adequate to explain these reactions as collisions don't dictate the reaction rate.
04

Generalizing Collision Theory for Any Order Reactions

Collision theory doesn't explain all reaction orders, especially those that involve complex mechanisms or are zero-order. It is most accurate for simple reactions in the gas phase where clear collisions between molecules can be envisioned.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

First Order Reactions
In the realm of chemical kinetics, first order reactions depict a scenario where the reaction rate is directly proportional to the concentration of a single reactant. Think of it as a one-on-one interaction, where the fate of the reaction hinges on one key player. The mathematical beauty of first order reactions lies in their simplicity, as the rate of reaction can be expressed by the equation: \(\text{rate} = k[\text{A}]\), where \(k\) is the rate constant and \(\text{A}\) refers to the reactant's concentration.

Collision theory shines when explaining first order reactions because it focuses on the single reacting species. When viewed through the lens of collision theory, these simple reactions suggest that the number of effective collisions per unit time is the maestro conducting the symphony of reactants turning into products. This is why, as part of our educational mission, we emphasize the practicality of collision theory in understanding the nuances of single reactant reactions.
Bimolecular Reactions
Bimolecular reactions are the dance of two molecules, choreographed by the laws of probability and energy. They are second-order reactions, hinging on the chance encounter and subsequent interaction between two reactant molecules. The reaction rate can be elucidated through the relation: \(\text{rate} = k[\text{A}][\text{B}]\), with \(k\) as the rate constant, and \(\text{A}\) and \(\text{B}\) representing the concentrations of the two reactants.

Delving deeper, collision theory does an excellent job of demystifying bimolecular reactions by proposing that for a product to emerge, a successful collusion is a must - not just any casual bump in the road, but one where the actors collide with enough energy to surpass the activation barrier and with a precision in orientation that permits the bonds to rearrange.
Reaction Rate
The reaction rate is the velocity at which a chemical reaction proceeds toward its final equilibrium. It is a central concept that captures the dynamism of chemical transformations. Often, students are curious about the factors influencing how briskly reactants turn into products. The rate is impacted by several factors: concentration of reactants, temperature, surface area, and the presence of a catalyst.

To convey the concept of reaction rate, you could visualize a rush hour traffic flow - the higher the number of cars (reactants), the more interactions (collisions) occur, impacting the flow (reaction rate). However, not all vehicles contribute equally; just as in a reaction, certain reactant concentrations or the presence of a catalyst can accelerate the rate. By understanding how these factors affect the reaction, students can better grasp the pace of chemical change and predict the time required for a reaction to complete.
Chemical Kinetics
Chemical kinetics is the study of the speed or rate at which chemical reactions occur and the factors that influence this velocity. It's the scientific investigation of the race to equilibrium - the finish line where reactants and products exist in a stable ratio.

Why does this matter? In the context of collision theory, kinetics provides insight into the molecular-level narrative driving the transformations we observe in the lab or in nature. By venturing into this microscopic universe, students learn that not every collision has what it takes - there are energy thresholds and orientation requirements that must be met to transform reactants into products. Chemical kinetics is the conceptual toolset allowing aspiring scientists and curious learners alike to decode the mysteries of reaction mechanisms, control chemical processes, and ultimately innovate within fields such as pharmaceuticals, environmental science, and materials engineering.

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Most popular questions from this chapter

Two radioactive nuclides \(A\) and \(B\) have half-lives \(50 \mathrm{~min}\) and \(10 \mathrm{~min}\) respectively. A fresh sample contains the nuclide of \(B\) to be eight time that of \(A\). How much time should elapse so that the number of nuclides of \(A\) becomes double of \(B\) ? (a) 30 (b) 40 (c) 50 (d) 100

Which of the following relation is correct for \(k_{f}\) and \(k_{b}\) in an equilibrium process that contains equal moles of reactants and products. (a) \(k_{f}=k_{b}\) (b) \(k_{f}>k_{b}\) (c) \(k_{f}

The radiation from naturally occurring radioactive substance as seen atter derlection by a magnetic field in one direction are : (a) \(\alpha\) -rays (b) \(\beta\) -rays (c) both \(\alpha\) and \(\beta\) rays (d) either \(\alpha\) or \(\beta\) -rays

For a first order homogeneous gaseous reaction, \(A \longrightarrow 2 B+C\) then initial pressure was \(P_{i}\) while total pressure after time ' \(t\) ' was \(P_{t}\). The right expression for the rate constants \(k\) in terms of \(P_{i}, P_{t}\) and \(t\) is : (a) \(k=\frac{2.303}{t} \log \left(\frac{2 P_{i}}{3 P_{i}-P_{t}}\right)\) (b) \(k=\frac{2.303}{t} \log \left(\frac{2 P_{i}}{2 P_{t}-P_{i}}\right)\) (c) \(k=\frac{2.303}{t} \log \left(\frac{P_{i}}{P_{i}-P_{t}}\right)\) (d) none of these

In the presence of an acid, the initial concentration of cane sugar was reduced from \(0.20\) to \(0.10\) molar in 5 hours and from \(0.2\) to \(0.05\) molar in 10 hours. The reaction is of- (a) Zero order (b) First order (c) Second order (d) Third order

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