Warning: foreach() argument must be of type array|object, bool given in /var/www/html/web/app/themes/studypress-core-theme/template-parts/header/mobile-offcanvas.php on line 20

The equilibrium constant for the conversion of the axial to the equatorial conformation of methoxycyclohexane is 2.7.


  1. Given these data, which conformation is present in the larger amount at equilibrium?
  2. Is ΔG° for this process positive or negative?
  3. From the values in Table 6.3, approximate the size of ΔG°.

Short Answer

Expert verified

Answer

  1. Equatorial conformation of methoxycyclohexane will be present in higher concentrations at equilibrium.
  2. The ΔG° for this process is negative.
  3. The size of ΔG° lies in the range of 0 to -6.

Step by step solution

01

Step-by-Step SolutionStep 1: Direction of a chemical reaction

A reaction always proceeds in the direction of stable species i.e., a reaction proceeds forward or backward depending on the stability of the reactants and products.

The reaction proceeds forwards only if the products are stable.

02

Equilibrium constant (Keq)  and free energy change (ΔG°)

A chemical reaction favors the products if its equilibrium constant has a value greater than one.

For a feasible reaction, the free energy change is always negative.

03

The conformer is present in a larger amount

  1. For the given reaction, the equilibrium constant has a value higher than one that indicates that the reaction proceeds forward i.e., towards the direction of equatorial conformation of methoxycyclohexane.
  2. Therefore, at equilibrium equatorial methoxycyclohexane will be present in the larger amount.
  3. Since the reaction proceeds in the forward direction, theΔG°will have a negative value.
  4. TheΔG° value lies in the range of 0 to -6 kJ/mol.

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 Vaia!

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

Consider the following reaction: CH4+Cl··CH3+HCl.

a. Use curved arrows to show the movement of electrons.

b. Calculate H°using the bond dissociation energies in Table 6.2.

c. Draw an energy diagram assuming that Ea=16kJ/mol.

d. What is Eafor the reverse reaction (·CH3+HClCH4+Cl·)?

The following is a concerted, bimolecular reaction:CH3+NaCNCH3CN+NaBr.

a. What is the rate equation for this reaction?

b. What happens to the rate of the reaction if[CH3Br] is doubled?

c. What happens to the rate of the reaction if [NaCN] is halved?

d. What happens to the rate of the reaction if [CH3Br] and [NaCN] are both increased by a factor of five?

Homolysis of the indicated C-H bond in propene forms a resonance-stabilized radical.

  1. Draw the two possible resonance structures for this radical.
  2. Use half-headed curved arrows to illustrate how one resonance structure can be converted to the other.
  3. Draw a structure for the resonance hybrid.

For a reaction with Keq=0.8and Ea=80kJ/mol, decide which of the following statements is (are) true. Correct any false statement to make it true. Ignore entropy considerations. (a) The reaction is faster than a reaction with Keq=8and Ea=80kJ/mol. (b) The reaction is faster than a reaction with Keq=0.8and Ea=40kJ/mol. (c) G° for the reaction is a positive value. (d) The starting materials are lower in energy than the products of the reaction. (e) The reaction is exothermic.

Use full-headed or half-headed curved arrows to show the movement of electrons in each reaction.

a.

b.

c.

d.

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.

Sign-up for free