Integrated SequencePhysics Chemistry Organic Biology

Web Resources

Virtual Textbook of Organic Chemistry - Reaction Rates and Kinetics
Solid, basic introduction to rate expressions and reaction order.

Purdue University - Instantaneous Rates of Reaction and the Rate Law for a Reaction



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Special points of emphasis

Chemical Kinetics

Nuclear Physics

Chemical Kinetics is another subject for which conceptual understanding is much more important for the MCAT than plug-and-chug quantitative problem solving. Every MCAT has questions calling upon you to exercise conceptual reasoning using Chemical Kinetics principles. Passages involving the interpretation of laboratory data to infer reaction order is fairly common as are basic questions regarding enzyme kinetics and questions on 'kinetic versus thermodynamic control'.

There is one type of quantitative kinetics question, however, which is very common, involving simple problem solving using half-life for first order kinetics. Most often though, the context will be radioactive decay rather than a chemical process. Radioactive decomposition is an important example of a first-order reaction process.




Stoichiometry

Chemical Kinetics

Reactions of Alkyl Halides

The order of a reaction cannot be predicted from the overall stoichiometric equation. That bears repeating. The rate expression for the reaction will agree with the stoichiometric equation only if all species are present in stoichiometric ratio at the rate determining step of the reaction mechanism.

The reaction mechanism determines the rate expression, not the overall stoichiometry. If a reagent is not present at the rate determining step, its concentration will not appear in the rate expression.

Substitution and elimination reactions represent the quintessential example from organic chemistry of the impossibility of predicting the rate expression from stoichiometry without knowing the mechanism.

A common type of problem is to present reaction rate data varying the concentration of reagents. If the rate of the reaction varies when the concentrations of both the alkyl halide substrate and the nucleophile (base) are changed, the mechanism must be bimolecular (E2 or SN2). However, if only the concentration of alkyl halide appears to change reaction rate, the mechanism must be unimolecular (E1 or SN1).

The rate expressions of the bimolecular reactions contain concentration expressions for both alkyl halide and nucleophile (base), while with the unimolecular reactions, the rate expression contains only the concentration expression of the alkyl halide.








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