- 220.127.116.11: (a) The dipole moment of trans-1,3-dibromocyclobutane is 1.1 D. Exp...
- 18.104.22.168: Tell whether each of the following compounds is chiral. (a) cis-1,2...
Solutions for Chapter 7.5: CyClopentane, CyClobutane, and CyClopropane
Full solutions for Organic Chemistry | 6th Edition
A pattern of variation in the amount of light absorbed by a sample as a function of wavelength. (Section 23.5)
Element in which the 5f orbitals are only partially occupied. (Section 6.8)
Compounds containing a carbon-carbon triple bond.
A step in a chain reaction that involves destruction of reactive intermediates
changes of state
Transformations of matter from one state to a different one, for example, from a gas to a liquid. (Section 1.3)
A technique by which compounds are separated from each other based on a difference in the way they interact with the medium (the adsorbent) through which they are passed.
A three-dimensional shape that can be adopted by a compound as a result of rotation about single bonds.
A compound containing a cyano group and a hydroxyl group connected to the same carbon atom.
A technique for separating amino acids from each other based on a difference in pI values.
A process in a chemical reaction that occurs in a single step. An overall chemical reaction consists of one or more elementary reactions or steps. (Section 14.6)
A protein molecule that acts to catalyze specific biochemical reactions. (Section 14.7)
frequency factor (A)
A term in the Arrhenius equation that is related to the frequency of collision and the probability that the collisions are favorably oriented for reaction. (Section 14.5)
The nucleophile in a Michael reaction.
Compounds formed when hydrogen reacts with nonmetals and metalloids. (Section 22.2)
Polymers that are similar in structure to polyesters but with repeating carbonate groups (!O!CO2!) instead of repeating ester groups (!CO2!). polycyclic aromatic hydrocarbons
A compound with a weak bond that undergoes homolytic bond cleavage with great ease, producing radicals that can initiate a radical chain process.
A measure of the decrease in concentration of a reactant or the increase in concentration of a product with time. (Section 14.2)
The difference in energy between a resonance hybrid and the most stable of its hypothetical contributing structures in which electrons are localized on particular atoms and in particular bonds.
Sanger dideoxy method
A method developed by Frederick Sanger for sequencing DNA molecules
A compound containing an SRO bond that is flanked on both sides by R groups.