- Chapter 1:
- Chapter 10:
- Chapter 11:
- Chapter 12:
- Chapter 13:
- Chapter 14:
- Chapter 15:
- Chapter 16:
- Chapter 17:
- Chapter 18:
- Chapter 19:
- Chapter 2:
- Chapter 20:
- Chapter 21:
- Chapter 22:
- Chapter 23:
- Chapter 24:
- Chapter 25:
- Chapter 3:
- Chapter 4:
- Chapter 5:
- Chapter 6:
- Chapter 7:
- Chapter 8:
- Chapter 9:
Chemistry 11th Edition - Solutions by Chapter
Full solutions for Chemistry | 11th Edition
An object that lacks chirality; an object that has no handedness
A high-energy intermediate formed during the elimination-addition reaction that occurs between chlorobenzene and either NaOH (at high temperature) or NaNH2.
A substance (molecule or ion) that acts as a proton acceptor. (Section 16.2)
A semiconducting material formed from two or more elements. (Section 12.7)
A monosaccharide that, when written as a Fischer projection, has the !OH on its penultimate carbon to the right.
A compound containing two hydroxyl groups
A carbohydrate containing two monosaccharide units joined by a glycosidic bond.
A type of secondary structure of DNA molecules in which two anti parallel polynucleotide strands are coiled in a right-handed manner about the same axis
A reaction in which the enthalpy of the products is higher than the enthalpy of the reactants; a reaction in which heat is absorbed
A polymer constructed from a single type of monomer.
A term that refers to the rate of a reaction.
limiting reactant (limiting reagent)
The reactant present in the smallest stoichiometric quantity in a mixture of reactants; the amount of product that can form is limited by the complete consumption of the limiting reactant. (Section 3.7)
A method for converting an alkene to an alcohol. The alkene is treated with mercury(II) acetate followed by reduction with sodium borohydride.
parts per million (ppm)
The concentration of a solution in grams of solute per 106 (million) grams of solution; equals milligrams of solute per liter of solution for aqueous solutions. (Section 13.4)
A polymer in which each monomer unit is joined to the next by an amide bond, as, for example, nylon 66.
A polymer constructed from nucleotides linked together.
A unimolecular nucleophilic substitution reaction.
A substance dissolved in a solvent to form a solution; it is normally the component of a solution present in the smaller amount. (Section 4.1)
Valence Bond Theory
A model of bonding that places electron pairs between adjacent atoms to create bonds.
a !CH"CH2 group