- 188.8.131.52.22: Compare diffusion with effusion.
- 184.108.40.206.23: State Grahams law of effusion.
- 220.127.116.11.24: Estimate the molar mass of a gas that effuses at 1.6 times the effu...
- 18.104.22.168.25: Determine the molecular mass ratio of two gases whose rates of effu...
- 22.214.171.124.26: List the following gases in order of increasing average molecular v...
- 126.96.36.199.27: ANALYZIN G IN FOR MATION An unknown gas effuses at one-half the spe...
Solutions for Chapter 11.4: Diffusion andEffusion
Full solutions for Modern Chemistry: Student Edition 2012 | 1st Edition
Reactions that are characterized by the addition of two groups across a double bond. In the process, the pi (p) bond is broken.
Stereoisomeric cyclic hemiacetals of an aldose or ketose that differ from each other in their configuration at the anomeric carbon.
Atoms that lie in the same plane.
An ionic compound that is formed upon treatment of a primary amine with NaNO2 and HCl.
A molecule containing an !S!S! group
An element that forms two bonds, such as oxygen.
Two mirror-image molecules of a chiral substance. The enantiomers are nonsuperimposable. (Section 23.4)
In Diels-Alder reactions that produce bicyclic structures, the positions that are anti to the larger bridge.
A mixture of triglycerides that is semisolid or solid at room temperature.
A carbohydrate in which the !OH on its anomeric carbon is replaced by !OR
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 type of carbocation rearrangement that involves the migration of a hydride ion (H-).
A cyclic amide.
Points in a crystal all of which have identical environments. (Section 12.2)
London dispersion forces
Attractive forces between transient dipole moments, observed in alkanes.
The study of carbon-containing compounds, typically containing carbon–carbon bonds. (Section 2.9; Chapter 24:Introduction)
The ratio of the actual (experimental) yield of a product to its theoretical (calculated) yield, multiplied by 100. (Section 3.7)
retro Diels-Alder reaction
The reverse of a Diels-Alder reaction, achieved at high temperature. A cyclohexene derivative is converted into a diene and a dienophile.
A sodium or potassium salt of a fatty acid
Cleavage by heating
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