Draw the Lewis structure for HCN. Indicate the hybrid orbitals, and draw a picture showing all the bonds between the atoms, labeling each bond as \(\sigma\) or \(\pi .\)

Short Answer

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The Lewis structure for HCN is H-σ-C≡N, with a lone pair of electrons on C and a lone pair on N. The hybridization of C is sp2 and that of N is sp. The single bond between H and C is a σ bond, while the triple bond between C and N consists of 1 σ bond and 2 π bonds.

Step by step solution

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1. Drawing the Lewis structure for HCN

Step 1 is to determine the total number of valence electrons in the molecule: - Hydrogen (H) has 1 valence electron - Carbon (C) has 4 valence electrons - Nitrogen (N) has 5 valence electrons So, HCN has a total of 10 valence electrons. Next, we will place the atoms with the least electronegative element in the center. In HCN, Carbon has the least electronegativity, so it serves as the central atom. Now, we will connect the central atom with outer atoms (hydrogen and nitrogen) using a single bond (2 electrons for each bond). This will consume 4 of the 10 valence electrons. Then, we will distribute the remaining 6 electrons as lone pairs to achieve an octet for each atom, starting with outer atoms first (as H already satisfied with 2 electrons). Nitrogen will have one lone pair of electrons (2 electrons), and Carbon will have one lone pair of electrons (2 electrons). This completes the distribution of all valence electrons.
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2. Identify hybrid orbitals

To identify hybrid orbitals on Carbon and Nitrogen, we will count the number of electron groups around each atom (lone pairs, single bonds, double bonds, or triple bonds). - Carbon has 3 electron groups: 1 single bond to H, 1 lone pair, and 1 triple bond to N. This corresponds to sp2 hybridization. - Nitrogen has 3 electron groups: 1 triple bond to C and 1 lone pair. This corresponds to sp hybridization.
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3. Draw a picture showing all the bonds, and label each bond as σ or π

Now, let's draw the complete structure of HCN by showing all the bonds and labeling them as σ or π. - There is a single bond between Hydrogen and Carbon, which is a σ bond. - The triple bond between Carbon and Nitrogen consists of 1 σ bond and 2 π bonds. The complete structure will look like this: H-σ-C≡N with a lone pair of electrons on C and a lone pair on N. The triple bond between C and N shows that there are 1 σ bond and 2 π bonds. The hybridization of C is sp2, and N is sp.

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Most popular questions from this chapter

The diatomic molecule OH exists in the gas phase. OH plays an important part in combustion reactions and is a reactive oxidizing agent in polluted air. The bond length and bond energy have been measured to be 97.06 \(\mathrm{pm}\) and 424.7 \(\mathrm{kJ} / \mathrm{mol}\) respectively. Assume that the OH molecule is analogous to the HF molecule discussed in the chapter and that the MOs result from the overlap of a \(p_{z}\) orbital from oxygen and the 1\(s\) orbital of hydrogen (the O-H bond lies along the z axis). a. Draw pictures of the sigma bonding and antibonding molecular orbitals in OH. b. Which of the two MOs has the greater hydrogen 1\(s\) character? c. Can the 2\(p_{x}\) orbital of oxygen form MOs with the 1\(s\) orbital of hydrogen? Explain. d. Knowing that only the 2\(p\) orbitals of oxygen interact significantly with the 1\(s\) orbital of hydrogen, complete the MO energy-level diagram for OH. Place the correct number of electrons in the energy levels. e. Estimate the bond order for OH. f. Predict whether the bond order of \(\mathrm{OH}^{+}\) is greater than, less than, or the same as that of OH. Explain.

In Exercise 95 in Chapter 8 , the Lewis structures for benzene \(\left(\mathrm{C}_{6} \mathrm{H}_{6}\right)\) were drawn. Using one of the Lewis structures, estimate \(\Delta H_{\mathrm{f}}^{\circ}\) for $\mathrm{C}_{6} \mathrm{H}_{6}(g)$ using bond energies and given that the standard enthalpy of formation of \(\mathrm{C}(g)\) is 717 $\mathrm{kJ} / \mathrm{mol}$ . The experimental \(\Delta H_{\mathrm{f}}^{\circ}\) value of $\mathrm{C}_{6} \mathrm{H}_{6}(g)\( is 83 \)\mathrm{kJ} / \mathrm{mol} .$ Explain the discrepancy between the experimental value and the calculated $\Delta H_{\mathrm{f}}^{\circ}\( value for \)\mathrm{C}_{6} \mathrm{H}_{6}(g)$

Place the species \(\mathrm{B}_{2}^{+}, \mathrm{B}_{2},\) and \(\mathrm{B}_{2}^{-}\) in order of increasing bond length and increasing bond energy.

Do lone pairs about a central atom affect the hybridization of the central atom? If so, how?

Consider three molecules: A, \(\mathrm{B},\) and \(\mathrm{C}\) . Molecule \(\mathrm{A}\) has a hybridization of \(s p^{3} .\) Molecule \(\mathrm{B}\) has two more effective pairs (electron pairs around the central atom) than molecule A. Molecule C consists of two \(\sigma\) bonds and two \(\pi\) bonds. Give the molecular structure, hybridization, bond angles, and an example for each molecule.

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