The incomplete Lewis structure below shows all the atoms and sigma bonds for a particular molecule, but nothing else. The molecule has a net charge of +1. Fill in any missing electrons to create the best Lewis structure for the molecule. Make sure to include any non-zero formal charges. HH \/ C ※ H N· HH .F ☑

Successive substitution of F atoms for H atoms in the molecule NH3 produces the molecules NH2F, NHF2, and NF3. a. Draw Lewis structures for each of the four molecules. b. Using VSEPR theory, predict the geometry of each of the four molecules. c. Specify the polarity (polar or nonpolar) for each of the four molecules.

The n-propyl cation can be formed from a molecule such as When the C–Cl bond is broken so that both electrons leave with Cl, the fragments formed are The carbon atom that had been attached to Cl is now sharing ____ electron pairs. In each shared pair the carbon atom owns ____ electron. The number of electrons that belong to carbon is ____. The formal charge on the carbon atom is ____. The correct Lewis structure for the n-propyl cation is

A common trait of simple organic compounds is to have Lewis structures where all atoms have a formal charge of zero. Consider the following incomplete Lewis structure for an organic compound called methyl cyanoacrylate, the main ingredient in Super Glue. Draw a complete Lewis structure for methyl cyanoacrylate in which all atoms have a formal charge of zero.

Best Lewis Formula and Molecular Geometry A student writes the Lewis electron-dot formula for the carbonate anion, CO32, as a Does this Lewis formula obey the octet rule? Explain. What are the formal charges on the atoms? Try describing the bonding for this formula in valence bond terms. Do you have any difficulty doing this? b Does this Lewis formula give a reasonable description of the electron structure, or is there a better one? If there is a better Lewis formula, write it down and explain why it is better. c The same student writes the following resonance description for CO2: Is there something wrong with this description? (What would you predict as the geometries of these formulas?) d Is one or the other formula a better description? Could a value for the dipole moment help you decide? e Can you write a Lewis formula that gives an even better description of CO2? Explain your answer.

Consider the following compounds: CO2, SO2, KrF2, SO3, NF3, IF3, CF4, SF4, XeF4, PF5, TF5, and SCl6. These 12 compounds are all examples of different molecular structures. Draw the Lewis structures for each and predict the molecular structures. Predict the bond angles and the polarity of each. (A polar molecule has a net dipole moment, while a nonpolar molecule does not.) See Exercises 25 and 26 for the molecular structures based on the trigonal bipyramid and the octahedral geometries.

Formamide, HC(O)NH2, is prepared at high pressures from carbon monoxide and ammonia, and serves as an industrial solvent (the parentheses around the O indicate that it is bonded only to the carbon atom and that the carbon atom is also bonded to the H and the N atoms). Two resonance forms (one with formal charges) can be written for formamide. Write both resonance structures, and predict the bond angles about the carbon and nitrogen atoms for each resonance form. Are they the same? Describe how the experimental determination of the HNH bond angle could be used to indicate which resonance form is more important.

How many electron dots should appear in the Lewis structures for each of the following polyatomic ions? a. ClO b. ClO2 c. S22 d. NH4+

a. How many sticks did you need to make the skeleton structure?____________ b. How many sticks are left over? ____________ If your model is to obey the octet rule, each ball must have four sticks in it except for hydrogen atom balls, which need and can only have one. Each atom in an octet rule species is surrounded by four pairs of electrons. c. How many holes remain to be filled? ____________ Fill them with the remaining sticks, which represent nonbonding electron pairs. Draw the complete Lewis structure for NH2Cl using lines for bonds and pairs of dots for nonbonding electrons.

The study of carbon-containing compounds and their properties is called organic chemistry. Besides carbon atoms, organic compounds also can contain hydrogen, oxygen, and nitrogen atoms (as well as other types of atoms). A common trait of simple organic compounds is to have Lewis structures where all atoms have a formal charge of zero. Consider the following incomplete Lewis structure for an organic compound called histidine (an amino acid), which is one of the building blocks of proteins found in our bodies: Draw a complete Lewis structure for histidine in which all atoms have a formal charge of zero.