Concept explainers
When a proton becomes bonded to diethyl ether,
In this 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 oxygen is ____. The formal charge on oxygen is ____. The correct Lewis structure for the conjugate acid of diethyl ether is
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Chapter 1 Solutions
Pushing Electrons
- Write 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_forwardThe 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 isarrow_forwardSuccessive 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.arrow_forward
- 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.arrow_forwardWrite 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_forward
- 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+arrow_forwardDraw Lewis structures for the following species. (The skeleton is indicated by the way the molecule is written.) (a) Cl2CO (b) H3C—CN (c) H2C—CH2arrow_forwardTwo different molecules have the formula C2H6O. One of the molecules has the oxygen atom bonded to both carbon atoms. The other molecule has the oxygen atom bonded to only one carbon atom while both carbon atoms are bonded to each other. Write Lewis structures for both of these compounds.arrow_forward
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