The C ≡ N triple bond in acetonitrile has a dipole moment of about 3.6Dand a bond length of about 1.16Å. Calculate the amount of charge separation in this bond. How important is the charge separated resonance form in the structure of acetonitrile?

Short Answer

Expert verified

Amount of charge separation is δ=0.6465e .

There is 64.65% of the charge separated resonance structure in resonance equilibrium.

Step by step solution

01

Bond dipole moment

The polarity of an individual bond is measured as its dipole moment (μ) which can be defined as μ=δ × d, where the amount of charge at either end of the dipole is represented by δ and the distance between the charges is represented by d . When common units are used, it can be written as:

μ (in debyes) =4.8 × δ(electroncharge) × d(in angstroms) .

02

Resonance structures

A single structural formula sometimes cannot explain all the properties of a compound that is given. In such cases, the compound may be represented by two or more structural formulae which differ from each other only in the arrangement of electrons. None of this structural formula alone can explain all the observed properties of the compound. The compound is then said to show resonance. The various structures are known as resonating structures.

03

Calculation of charge separation and relative importance of the resonating form

As per given data,

Dipole moment (μ) = 3.6D

Distance between the charges(d )= 1.16 Å

Now,

μ (in debyes) =4.8 × δ(electroncharge) × d(in angstroms)

⟹ 3.6D = 4.8 × δ × 1.16 Å

⟹ δ = 3.6 ∕ 4.8 × 1.16

⟹ δ = 3.6 ∕ 5.568

⟹ δ = 0.6465 e

The amount δ of charge separation is about 0.6465 e (electronic charge).

The amount of charge separation is found to be 0.6465 e which implies that there is 64.65% of the charge separated resonance structure in resonance equilibrium.

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Most popular questions from this chapter

Question: The pKa of ascorbic acid (vitamin C, page 9) is 4.17 , showing that it is lightly more acidic than acetic acid (CH3COOH, pKa = 4.74).

(a)Show four different conjugate bases that would be formed by deprotonation of the four different OH groups in ascorbic acid.

(b) Compare the stabilities of these four conjugate bases, and predict which OH group of ascorbic acid is the most acidic.

(c) Compare the most stable conjugate base of ascorbic acid with the conjugate base of acetic acid, and suggest why these two compounds have similar acidities, even though ascorbic acid lacks the carboxylic acid (COOH) group

All of the following compounds can react with acids. Without using a table of acidities, rank them in order of increasing acidity. Explain your ranking.

(a)

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(e)

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(a) alkane

(b) alkene

(c) alkyne

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(g) aldehyde

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(j) ester

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Ammonia appears in Table 2-2 as both an acid and a conjugate base.

  1. Explain how ammonia can act as both an acid and a base. Which of these roles does it commonly fill in aqueous medium?
  2. Show how water can serve both as an acid and a base.
  3. CalculateKaand pKa for the hydronium ion, H3O+ .
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Consider the type of orbitals involved, and rank the following nitrogen compounds in order of decreasing basicity. Give the structure of their conjugate acids; and estimate their pKas from similar compounds in Appendix 4. Rank the conjugate acids in order of increasing acidity. (Hint: These two orders should be the same!)

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