Concept explainers
Methanol,
This time we use the curved arrow to signify bond making. Now a pair of unshared electrons on oxygen is pushed toward the region between the oxygen atom and the hydrogen ion. It becomes an
In the resulting structure the oxygen atom owns one electron from each of ____ shared pairs and two electrons from ____ unshared pair. The total number of electrons that belong to the oxygen atom is ____. Oxygen is a Group ____ element. Since the number of electrons that the oxygen atom owns in this structure is one fewer that it would have in the neutral, unbonded state, the charge on oxygen is ____. The correct Lewis structure for the conjugate acid of methanol is
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Once again charge is conserved. Joining a neutral molecule and a cation must yield a cation. Again the formal charge distribution on the resulting ion is predictable from the arrow. Electrons are pushed away from the oxygen atom, leaving it with a positive charge. Electrons are pushed toward the hydrogen ion, neutralizing its erstwhile positive charg.
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Chapter 1 Solutions
Pushing Electrons
- Chloromethane has the Lewis structure _______________________________ The carbon atom is sharing 4 electron pairs. In each shared pair the carbon atom “owns” 1 electron. The number of electrons that “belong” to carbon is ___. Carbon, being a Group ___ element would have 4 , outer shell electrons in the unbonded, neutral state. Therefore, the carbon atom in chloromethane has a formal charge of zero.arrow_forwardWhat is the formal charge on the indicated atom in each of the following species? (a) sulfur in SO2 (b) nitrogen in N2H4 (c) each oxygen atom in ozone, O3arrow_forwardWrite all resonance structures of chlorobenzene, C6H5Cl, a molecule with the same cyclic structure as benzene. In all structures, keep the CCl bond as a single bond. Which resonance structures are the most important?arrow_forward
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- Write Lewis structures for these ions. Show all valence electrons and all formal charges. (a) Amide ion, NH2 (b) Bicarbonate ion, HCO3 (c) Carbonate ion, CO32 (d) Nitrate ion, NO3 (e) Formate ion, HCOO (f) Acetate ion, CH3COOarrow_forwardFormamide, 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.arrow_forwardThree resonance forms can be drawn for the molecule N2O. Which resonance form is likely to more closely resemble the structure of this molecule? (a) (b) (c)arrow_forward
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