- Lesson 82.1: Explain how you would prepare a solution of sucrose with a molarity...
- Lesson 82.2: How are mass of solute, moles of solute, and volume of solution rel...
- Lesson 82.3: How many grams of solute do you need to make 1 L of each of the sol...
- Lesson 82.4: Copy this table and complete it for solutions of glucose, C6H12O6. ...
- Lesson 82.5: What volume of each of these solutions would contain 58.44 g of NaC...
- Lesson 82.6: How many grams of fructose, C6H12O6, are in 1 L of soft drink if th...
- Lesson 82.7: Which is more concentrated: a 1.0 L solution with 20 g of sucrose, ...
- Lesson 82.8: The Environmental Protection Agency has set the upper limit for fl ...
Solutions for Chapter Lesson 82: Preparing Solutions
Full solutions for Living by Chemistry | 2nd Edition
An object that lacks chirality; an object that has no handedness
activated complex (transition state)
The particular arrangement of atoms found at the top of the potential-energy barrier as a reaction proceeds from reactants to products. (Section 14.5)
Compounds consisting of a single ring containing a fully conjugated p system. Benzene is annulene.
Bond dipole moment
A measure of the polarity of a covalent bond. The product of the charge on either atom of a polar bond times the distance between the atoms
A rule that states that it is not possible for a bridgehead carbon of a bicyclic system to possess a carbon carbon double bond if it involves a trans p bond being incorporated in a ring comprised of fewer than eight atoms.
Cis, trans isomers
Stereoisomers that have the same connectivity but a different arrangement of their atoms in space as a result of the presence of either a ring or a carboncarbon double bond.
The number of adjacent atoms to which an atom is directly bonded. In a complex the coordination number of the metal ion is the number of donor atoms to which it is bonded. (Sections 12.37 and 24.2)
crossed aldol reaction
An aldol reaction that occurs between different partners.
The left side of an NMR spectrum.
A bimolecular b-elimination reaction.
A chemical formula that shows the kinds of atoms and their relative numbers in a substance in the smallest possible whole-number ratios. (Section 2.6)
A reaction in which the Gibbs free energy of the products is higher than that of the reactants. The position of equilibrium for an endergonic reaction favors starting materials
A fi ve-membered cyclic form of a monosaccharide.
The catalyst system and conditions of temperature and pressure developed by Fritz Haber and coworkers for the formation of NH3 from H2 and N2. (Section 15.2)
heat of vaporization
The enthalpy change, ?H, for vaporization of a liquid. (Section 11.4)
In 1H NMR spectroscopy, the area under a signal indicates the number of protons giving rise to the signal.
A monosaccharide that, when written as a Fischer projection, has the !OH on its penultimate carbon to the left.
A compound capable offunctioning as an electron pair donor.
Secondary structure of nucleic acids
The ordered arrangement of nucleic acid strands
A polymer with alternating R and S confi gurations at the chiral centers along its chain, as, for example, syndiotactic polypropylene