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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?

Short Answer

Expert verified
(a) To satisfy the octet rule, draw a Lewis structure with S as the central atom, single bonds between S and each of the 4 O atoms, and single bonds between 2 O atoms and their respective H atoms, with the remaining 24 electrons distributed around the O atoms. In this structure, all atoms obey the octet rule. (b) To minimize formal charges, create double bonds between S and 2 of the O atoms while keeping the single bonds between the other 2 O atoms and their respective H atoms. In this structure, all formal charges are 0, satisfying both the octet rule and minimizing formal charges.

Step by step solution

01

Calculate Total Valence Electrons

First, we need to find the total number of valence electrons in H2SO4. The valence electrons for each element are: H = 1, S = 6, and O = 6. In sulfuric acid, there are 2 H atoms, 1 S atom, and 4 O atoms. Therefore, the total valence electrons are: Total Valence Electrons = (2 x 1) + (1 x 6) + (4 x 6) = 2 + 6 + 24 = 32
02

Place Central Atom and Identify Bonding Atoms

Sulfur (S) is the central atom as it has the lowest electronegativity in the compound. The outer atoms are the oxygen (O) and hydrogen (H) atoms. Place the S atom in the center and connect it with 4 O atoms using single bonds. Since H atoms can only bond once, connect each of the 2 remaining O atoms with 1 H atom each.
03

Distribute Remaining Electrons

To satisfy the octet rule, distribute the remaining electrons to the outer atoms (O and H). Currently, there are 4 single bonds, 1 between S and each O atom. A single bond accounts for 2 electrons, so 8 electrons are already used in the structure. There are 32 - 8 = 24 electrons left to distribute. Place the remaining 24 electrons around the outer O atoms (6 electrons around each O atom). Since H atoms can only have two electrons around them, there is no need to distribute the electrons to H. (a) At this point, all atoms satisfy the octet rule: S: 6 valence electrons + 4 single bonds = 6 + (4 x 2) = 14 electrons O: 6 valence electrons + 1 single bond + 6 non-bonding electrons = 6 + 2 + 6 = 14 electrons H: 1 valence electron + 1 single bond = 1 + 2 = 2 electrons
04

Calculate Formal Charges

Next, we calculate the formal charge on each atom: Formal Charge = Valence Electrons - (Non-bonding Electrons + 0.5 x Bonding Electrons) For the S atom: Formal Charge = 6 - (0 + 0.5 x 8) = 6 - 4 = +2 - For the O atoms bonded to the H atoms (we have two of them): Formal Charge = 6 - (6 + 0.5 x 2) = 6 - 7 = -1 - For the other O atoms (we have two of them): Formal Charge = 6 - (6 + 0.5 x 2) = 6 - 7 = -1 (b) To minimize the formal charge, create double bonds between S and 2 of the O atoms: S = O \\ O-S-O // O Now, the formal charges become 0 for all atoms: For the S atom: Formal Charge = 6 - (0 + 0.5 x 12) = 6 - 6 = 0 For all O atoms: Formal Charge = 6 - (4 + 0.5 x 4) = 6 - 6 = 0 Thus, the Lewis structure that satisfies the octet rule and minimizes the formal charge is the one with double bonds between S and two O atoms and single bonds between S and the remaining O atoms, each of which is bonded to an H atom.

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Key Concepts

These are the key concepts you need to understand to accurately answer the question.

Chemical Bonding
Understanding chemical bonding is fundamental to grasping the structure of sulfuric acid, \( \mathrm{H}_{2}\mathrm{SO}_{4} \). Chemical bonds form when atoms share or transfer electrons to achieve a stable electron configuration, usually the octet rule for many elements. In the Lewis structure of \( \mathrm{H}_{2}\mathrm{SO}_{4} \), sulfur bonds with oxygen and hydrogen atoms to fulfill this stable configuration.

At the core of sulfuric acid's structure is the element sulfur (S), which acts as a central atom. It is surrounded by oxygen (O) atoms, two of which are attached to hydrogen (H) atoms. We know that electron sharing occurs through the formation of covalent bonds. Initially, each S-O bond is a single bond; however, to minimize formal charge, some of these bonds become double bonds. This is a key characteristic that affects the shape and reactivity of the molecule. Double bonds are stronger and shorter than single bonds and play a critical role in the overall stability of the molecule.
Valence Electrons
Valence electrons are the electrons in the outermost shell of an atom that can participate in the formation of chemical bonds. In the exercise, the number of valence electrons is used to construct the Lewis structure of sulfuric acid. Hydrogen has 1 valence electron, sulfur has 6, and oxygen has 6. The summation of these electrons gives us the total to work with—32 valence electrons for \( \mathrm{H}_{2}\mathrm{SO}_{4} \).

The arrangement of these electrons is the first step in drawing our Lewis structure. Sulfuric acid is unique because while hydrogen generally forms single bonds, sulfur and oxygen can form multiple bond types. In structuring the molecule, it's essential to place these valence electrons not only to form bonds but also to fill the octets of the oxygen atoms, adhering to the octet rule. The remaining electrons are assigned as lone pairs or part of double bonds to minimize the formal charge and satisfy the octet requirement for each atom.
Formal Charge
Formal charge is a bookkeeping tool used in chemistry to determine the charge distribution within a molecule. The lower the formal charge, the more stable the molecule. To compute the formal charge, the formula is:\[\text{Formal Charge} = \text{Valence Electrons} - (\text{Non-bonding Electrons} + 0.5 \times \text{Bonding Electrons})\]

In the example of \( \mathrm{H}_{2}\mathrm{SO}_{4} \), we've seen that initially, the sulfur atom had a formal charge of +2, and the oxygen atoms had a formal charge of -1. To achieve a more stable structure with lower formal charges, we rearrange electrons to form double bonds. This reduces the formal charge on sulfur to 0, while also bringing the oxygen atoms' formal charges to 0. A Lewis structure that minimizes formal charge tends to be the most representative of the molecule's actual electronic structure, and this consideration is crucial when predicting the behavior and reactivity of molecules.

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Most popular questions from this chapter

True or false: (a) The \(\mathrm{C}-\) Cbonds in benzene are all the same length and correspond to typical single \(\mathrm{C}-\mathrm{Cbond}\) lengths. (b) The \(\mathrm{C}-\mathrm{C}\) bond in acetylene, HCCH, is longer than the average \(\mathrm{C}-\mathrm{C}\) bond length in benzene.

A common form of elemental phosphorus is the tetrahedral \(\mathrm{P}_{4}\) molecule, where all four phosphorus atoms are equivalent: At room temperature phosphorus is a solid. (a) Are there any lone pairs of electrons in the \(\mathrm{P}_{4}\) molecule? (b) How many \(\mathrm{p}-\mathrm{p}\) bonds are there in the molecule? (c) Draw a Lewis structure for a linear \(P_{4}\) molecule that satisfies the octet rule. Does this molecule have resonance structures? (d) On the basis of formal charges, which is more stable, the linear molecule or the tetrahedral molecule?

(a) Use Lewis symbols to represent the reaction that occurs between Ca and F atoms. (b) What is the chemical formula of the most likely product? (c) How many electrons are transferred? ( \(\mathbf{d} )\) Which atom loses electrons in the reaction?

Energy is required to remove two electrons from Ca to form \(\mathrm{Ca}^{2+},\) and energy is required to add two electrons to \(\mathrm{O}\) to form \(\mathrm{O}^{2-} .\) Yet \(\mathrm{CaO}\) is stable relative to the free elements. Which statement is the best explanation? (a) The lattice energy of CaO is large enough to overcome these processes. (b) CaO is a covalent compound, and these processes are irrelevant. (c) CaO has a higher molar mass than either Ca or O. (d) The enthalpy of formation of CaO is small. (e) CaO is stable to atmospheric conditions.

Arrange the bonds in each of the following sets in order of increasing polarity: (a) \(\mathrm{C}-\mathrm{F}, \mathrm{O}-\mathrm{F}, \mathrm{Be}-\mathrm{F}\) ; (b) \(\mathrm{O}-\mathrm{Cl}, \mathrm{S}-\mathrm{Br}, \mathrm{C}-\mathrm{P} ;(\mathbf{c}) \mathrm{C}-\mathrm{S}, \mathrm{B}-\mathrm{F}, \mathrm{N}-\mathrm{O}\)

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