- Chapter 1: Introduction to Chemistry
- Chapter 10: The Mole
- Chapter 11: Stoichiometry
- Chapter 12: States of Matter
- Chapter 13: Gases
- Chapter 14: Mixtures and Solutions
- Chapter 15: Energy and Chemical Change
- Chapter 16: Reaction Rates
- Chapter 17: Chemical Equilibrium
- Chapter 18: Acids and Bases
- Chapter 19: Redox Reactions
- Chapter 2: Analyzing Data
- Chapter 20: Electrochemistry
- Chapter 21: Hydrocarbons
- Chapter 22: Substituted Hydrocarbons and Their Reactions
- Chapter 23: The Chemistry of Life
- Chapter 24: Nuclear Chemistry
- Chapter 3: Matter Properties and Changes
- Chapter 4: The Structure of the Atom
- Chapter 5: Electrons in Atoms
- Chapter 6: The Periodic Table and Periodic Law
- Chapter 7: Ionic Compounds and Metals
- Chapter 8: Covalent Bonding
- Chapter 9: Chemical Reactions
Chemistry: Matter & Change 1st Edition - Solutions by Chapter
Full solutions for Chemistry: Matter & Change | 1st Edition
ISBN: 9780078746376
Since problems from 24 chapters in Chemistry: Matter & Change have been answered, more than 248257 students have viewed full step-by-step answer. Chemistry: Matter & Change was written by and is associated to the ISBN: 9780078746376. This textbook survival guide was created for the textbook: Chemistry: Matter & Change, edition: 1. This expansive textbook survival guide covers the following chapters: 24. The full step-by-step solution to problem in Chemistry: Matter & Change were answered by , our top Chemistry solution expert on 11/10/17, 05:56PM.
-
amine
Compounds containing a nitrogen atom that is connected to one, two, or three alkyl or aryl groups.
-
boat conformation
A conformation of cyclohexane in which all bond angles are fairly close to 109.5° and many hydrogen atoms are eclipsing each other.
-
boiling point.
The temperature at which the vapor pressure of a liquid is equal to the external atmospheric pressure. (11.8)
-
chelate effect
The generally larger formation constants for polydentate ligands as compared with the corresponding monodentate ligands. (Section 23.3)
-
chemical equation.
An equation that uses chemical symbols to show what happens during a chemical reaction. (3.7)
-
concentration
The quantity of solute present in a given quantity of solvent or solution. (Section 4.5)
-
E
For alkenes, a stereodescriptorthat indicates that the two priority groups are on opposite sides of the p bond.
-
electromotive force (emf)
A measure of the driving force, or electrical pressure, for the completion of an electrochemical reaction. Electromotive force is measured in volts: 1 V = 1 J>C. Also called the cell potential. (Section 20.4)
-
heat of combustion
The heat given off during a reaction in which an alkane reacts with oxygen to produce CO2 and water.
-
Hydrogenolysis
Cleavage of a single bond by H2, most commonly accomplished by treating a compound with H2 in the presence of a transition metal catalyst.
-
internal alkyne
A compound with the structure R!C#C!R, where each R group is not a hydrogen atom.
-
inversion of configuration
During a reaction, when the configuration of a chirality center is changed.
-
molecular hydrides
Compounds formed when hydrogen reacts with nonmetals and metalloids. (Section 22.2)
-
Nonpolar covalent bond
A covalent bond between atoms whose difference in electronegativity is less than approximately 0.5.
-
Nucleophile
From the Greek meaning nucleus-loving. Any species that can donate a pair of electrons to form a new covalent bond; alternatively, a Lewis base
-
orbital
An allowed energy state of an electron in the quantum mechanical model of the atom; the term orbital is also used to describe the spatial distribution of the electron. An orbital is defined by the values of three quantum numbers: n, l, and ml (Section 6.5)
-
proteins
Polypeptide chains comprised of more than 40 or 50 amino acids.
-
reactant
A starting substance in a chemical reaction; it appears to the left of the arrow in a chemical equation. (Section 3.1)
-
Thiol
A compound containing an !SH (sulfhydryl) group bonded to an sp3 -hybridized carbon.
-
weak activators
Groups that weakly activate an aromatic ring toward electrophilic aromatic substitution, thereby enhancing the rate of the reaction.