- Lesson 30.1: What is the HONC 1234 rule?
- Lesson 30.2: Explain why one molecular formula can represent more than one struc...
- Lesson 30.3: Use the HONC 1234 rule to create possible structural formulas for m...
- Lesson 30.4: Is each structural formula correct according to the HONC 1234 rule?...
- Lesson 30.5: Think about how molecules might interact with your nose. Why do you...
Solutions for Chapter Lesson 30: Bonding Tendencies
Full solutions for Living by Chemistry | 2nd Edition
A summary of the results of many possible displacement reactions. (4.4)
An amine in which nitrogen is bonded only to alkyl groups.
Compounds containing a nitrogen atom that is connected to one, two, or three alkyl or aryl groups.
When applying Woodward-Fieser rules, the groups attached to the chromophore.
An equilibrium property measured by the position of equilibrium in an acid-base reaction, as, for example, the acid-base reaction between ammonia and water.
The distance between the centers of two bonded atoms. (Section 8.3)
A binary compound of carbon with a metal or metalloid. (Section 22.9)
A process by which molecular oxygen is used to convert food into CO2, water, and energy.
A polydentate ligand that is capable of occupying two or more sites in the coordination sphere. (Section 23.3)
A chemical reaction in which two or more substances combine to form a single product. (Section 3.2)
A chemical reaction that proceeds with evolution of heat and usually also a flame; most combustion involves reaction with oxygen, as in the burning of a match. (Section 3.2)
Any substituent on a benzene ring that causes the rate of electrophilic aromatic substitution to be lower than that for benzene.
deoxyribonucleic acid (DNA)
A polynucleotide in which the sugar component is deoxyribose. (Section 24.10)
A semiconducting material composed of just one element. (Section 12.7)
A conformation that exhibits a gauche interaction.
Chemistry that promotes the design and application of chemical products and processes that are compatible with human health and that preserve the environment. (Section 18.5)
A monosaccharide that, when written as a Fischer projection, has the !OH on its penultimate carbon to the left.
A diagram that shows the energies of molecular orbitals relative to the atomic orbitals from which they are derived; also called an energy-level diagram. (Section 9.7)
Polymers that are similar in structure to polyesters but with repeating carbonate groups (!O!CO2!) instead of repeating ester groups (!CO2!). polycyclic aromatic hydrocarbons
The general process of advancing scientific knowledge by making experimental observations and by formulating hypotheses, theories, and laws. (Section 1.3)