(a) Draw the best Lewis structure(s) for the nitrite ion, NO \(_{2}^{-}\) (b) With what allotrope of oxygen is it isoelectonic? (c) What would you predict for the lengths of the bonds in \(\mathrm{NO}_{2}^{-}\) relative to \(\mathrm{N}-\mathrm{O}\) single bonds and double bonds?

Short Answer

Expert verified
The nitrite ion (NO₂⁻) has two resonance structures: O-N=O and O=N-O. The isoelectronic allotrope of oxygen is ozone (O₃). The bond lengths in NO₂⁻ are shorter than in N-O single bonds but longer than in N=O double bonds due to the delocalized bonding having a bond order of approximately 1.5.

Step by step solution

01

(a) Drawing the Lewis Structure for NO₂⁻

To draw the Lewis structure for the nitrite ion, we need to consider the total number of valence electrons and arrange the atoms accordingly. 1. Count Valence Electrons: Nitrogen (N) has 5 valence electrons, Oxygen (O) has 6 valence electrons, and there is one additional electron due to the negative charge of the ion. So, the total number of valence electrons is (5 + 2*6 + 1) = 18. 2. Arrange the Atoms: Put the least electronegative atom in the center (N), and the remaining atoms (O) around it. Connect the central atom to surrounding atoms with single bonds. 3. Add Lone Pairs: Complete the octets for the surrounding atoms (O) by adding lone pairs. 4. Add Multiple Bonds: If the central atom (N) does not have a complete octet, create multiple bonds with one or more surrounding atoms. In the case of NO₂⁻, there are two possible resonance structures, which are equally important for the description of the bonding in the ion. The resulting two resonance structures can be represented as follows: O-N=O <-----> O=N-O
02

(b) Identifying the Isoelectronic Allotrope of Oxygen

An allotrope of oxygen that is isoelectronic with NO₂⁻ should have the same number of total electrons. Since NO₂⁻ has 5+6+6+1=18 electrons, the oxygen allotrope must also have 18 electrons. Ozone (O₃) is found to be isoelectronic with NO₂⁻, as each oxygen atom has 6 electrons, and hence O₃ has 3*6 = 18 electrons.
03

(c) Predicting the Bond Lengths in NO₂⁻ Relative to N-O Single and Double Bonds

Since NO₂⁻ has two resonance structures, O-N=O <-----> O=N-O, it shows that the N-O bonds are delocalized, which means they are somewhere between a single bond (N-O) and a double bond (N=O). A single bond (N-O) will typically be longer than a double bond (N=O), because there is only one shared pair of electrons in a single bond, causing less electrostatic attraction between the atoms. In NO₂⁻, the delocalized bonds mean that the electrons are shared over both N-O bonds, giving each bond a bond order of about 1.5. This partial double bond character will make the bond lengths in NO₂⁻ shorter than N-O single bonds, but longer than N=O double bonds.

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

Write electron configurations for the following ions, and determine which have noble-gas configurations: (a) \(\mathrm{Cd}^{2+}\) , \((\mathbf{b}) \mathrm{P}^{3-},(\mathbf{c}) \mathrm{Zr}^{4+},(\mathbf{d}) \mathrm{Ru}^{3+},(\mathbf{e}) \mathrm{As}^{3-},(\mathbf{f}) \mathrm{Ag}^{+}\)

Formic acid has the chemical formula HCOOH. It is a colorless liquid that has a density of 1.220 \(\mathrm{g} / \mathrm{mL}\) . (a) The carbon atom in formic acid is bound to one \(\mathrm{H}\) and both \(\mathrm{O}^{\prime}\) 's. Draw the Lewis structure for formic acid, showing resonance if present. (b) Formic acid can react with NaOH in aqueous solution to produce the formate ion, HCOO- . Write the balanced chemical equation for this reaction. (c) Draw the Lewis structure of the formate ion, showing resonance if present. (d) How many milliliters of a 0.100 M solution of NaOH would it take to completely react with 0.785 \(\mathrm{mL}\) of formic acid?

There are many Lewis structures you could draw for sulfuric acid, \(\mathrm{H}_{2} \mathrm{SO}_{4}\) (each \(\mathrm{H}\) is bonded to an O). (a) What Lewis structure(s) would you draw to satisfy the octet rule? (b) What Lewis structure(s) would you draw to minimize formal charge?

Which of the following statements about electronegativity is false? (a) Electronegativity is the ability of an atom in a molecule to attract electron density toward itself. (b) Electronegativity is the same thing as electron affinity. (c) The numerical values for electronegativity have no units. (d) Fluorine is the most electronegative element. (e) Cesium is the least electronegative element.

Some chemists believe that satisfaction of the octet rule should be the top criterion for choosing the dominant Lewis structure of a molecule or ion. Other chemists believe that achieving the best formal charges should be the top criterion. Consider the dihydrogen phosphate ion, \(\mathrm{H}_{2} \mathrm{PO}_{4}^{-}\) , in which the \(\mathrm{H}\) atoms are bonded to \(\mathrm{O}\) atoms. (a) What is the predicted dominant Lewis structure if satisfying the octet rule is the top criterion? (b) What is the predicted dominant Lewis structure if achieving the best formal charges is the top criterion?

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