/*! This file is auto-generated */ .wp-block-button__link{color:#fff;background-color:#32373c;border-radius:9999px;box-shadow:none;text-decoration:none;padding:calc(.667em + 2px) calc(1.333em + 2px);font-size:1.125em}.wp-block-file__button{background:#32373c;color:#fff;text-decoration:none} Q12P Under certain conditions, the br... [FREE SOLUTION] | 91Ó°ÊÓ

91Ó°ÊÓ

Under certain conditions, the bromination of cyclohexene follows an unusual rate law:

(a) What is the kinetic order with respect to cyclohexene?

(b) What is the kinetic order with respect to bromine?

(c) What is the kinetic order overall?

Short Answer

Expert verified

(a) First order.

(b) Second order.

(c) Third order.

Step by step solution

01

Rate equation

It may be defined as the relationship between the concentrations of the reactants and the observed reaction rate. Each reaction has its own rate equation which may be determined experimentally by altering the concentration of the reactants and then measuring the change in rate.

Consider a general reaction of the type: aA + bB→products

The reaction rate is usually proportional to the concentrations of the reactants [A] and [B] which are raised to powers and respectively. The rate expression can, then be written as:

rate =kr[A]a[B]b, where kr= rate constant.

02

Order of a reaction.

The order of a reaction may be defined as the sum of the exponents to which the concentration terms in the rate law are raised to express the observed rate of reaction.

From the general equation of the type: aA + bB → products, the rate expression can be written as, rate =kr [A]a[B]b .

a and b are called the orders of the reaction with respect to A and B. Depending on whether (a+b) is equal to 0,1,2 or 3, the reactions are said to be of zero order, first order, second order, and third order respectively.

03

Explanation

(a) From the rate equation, it is evident that the order with respect to cyclohexene is first order.

(b) From the rate equation , it is evident that the order with respect to bromine is second order.

(c) Order with respect to cyclohexene is first order and the order with respect to bromine is second order. Therefore, overall order is which is equal to 3 (third order).

Unlock Step-by-Step Solutions & Ace Your Exams!

  • Full Textbook Solutions

    Get detailed explanations and key concepts

  • Unlimited Al creation

    Al flashcards, explanations, exams and more...

  • Ads-free access

    To over 500 millions flashcards

  • Money-back guarantee

    We refund you if you fail your exam.

Over 30 million students worldwide already upgrade their learning with 91Ó°ÊÓ!

One App. One Place for Learning.

All the tools & learning materials you need for study success - in one app.

Get started for free

Most popular questions from this chapter

Iodination of alkanes using iodine (I2)is usually an unfavorable reaction. (See problem 4-17, for example). Tetraiodomethane (Cl4) can be used as the iodine source for iodination in the presence of a free-radical initiator such as hydrogen peroxide. Propose a mechanism (involving mildly exothermic propagation steps) for the following proposed reaction. Calculate the value of Δ±áfor each of the steps in your proposed mechanism.

The following bond-dissociation energies may be helpful:

The following reaction has a value ofΔ³Ò0= -2.1 k´³/³¾´Ç±ô â¶Ä‰(-0.50 â¶Ä‰k³¦²¹±ô/³¾´Ç±ô)

CH3µþ°ù â¶Ä‰+ â¶Ä‰H2³§â€‰â¶Ä‰â‡„ â¶Ä‰C±á3³§±á â¶Ä‰+ â¶Ä‰Hµþ°ù

(a) Calculate Keqat room temperature(250C) for this reaction as written.

(b)Starting with a1M solution of CH3Brand H2S, calculate the final concentrations of all four species at equilibrium.

(a) Draw a reaction-energy diagram for the following reaction:

The activation energy is 4 kJ/mol (1 kcal/mol), and the overall for the reaction is -110 kJ/mol (-27 kcal/mol).

(b) Give the equation for the reverse reaction.

(c) What is the activation energy for the reverse reaction?

Predict the ratios of products that result from chlorination of isopentane.(2-methylbutane)

In the presence of a small amount of bromine, cyclohexene undergoes the following light-promoted reaction:

(a) Propose a mechanism for this reaction.

(b) Draw the structure of the rate-limiting transition state.

(c) Use Hammond’s postulate to predict which intermediate most closely resembles this transition state.

(d) Explain why cyclohexene reacts with bromine much faster than cyclohexane, which must be heated to react.

See all solutions

Recommended explanations on Chemistry Textbooks

View all explanations

What do you think about this solution?

We value your feedback to improve our textbook solutions.

Study anywhere. Anytime. Across all devices.