- 5.4.9: Assign relative priorities to each set of substituents: a. iBr iI i...
- 5.4.10: Tamoxifen slows the growth of some breast tumors by binding to estr...
- 5.4.11: Draw and label the E and Z isomers for each of the following: a. CH...
- 5.4.12: Draw skeletal structures for each pair of isomers in .
- 5.4.13: Name each of the following:
- 5.4.14: Draw the structure of ( Z )-3-isopropyl-2-heptene.
- 5.4.15: Draw the isomers for the following compounds, and then name each on...
Solutions for Chapter 5.4: Naming Alkenes Using the E,Z System
Full solutions for Organic Chemistry | 7th Edition
Hydrocarbons having the general formula CnH2n12, where n 5 1,2, . . . . (24.2)
The compound CH2"C"CH2. Any compound that contains adjacent carbon-carbon double bonds; that is, any molecule that contains a C"C"C functional group.
amphoteric oxides and hydroxides
Oxides and hydroxides that are only slightly soluble in water but that dissolve in either acidic or basic solutions. (Section 17.5)
A polymer in which the repeating units contain chirality centers which are not arranged in a pattern (they have random configurations).
A conjugated diene or carbonyl is one in which the double bonds are separated by one single bond
A reaction involving loss of CO2, characteristic of compounds containing a carbonyl group that is beta to a COOH group.
A method for analyzing the sequence of amino acids in apeptide by removing one amino acid residue at a time and identifying each residue as it is removed.
gas chromatograph – mass spectrometer
A device used for the analysis of a mixture that contains several compounds.
Finely powdered palladium metal deposited on solid calcium carbonate that has been specially modifi ed with lead salts. Its particular use is as a catalyst for the reduction of an alkyne to a cis alkene
The mass of one mole of a substance in grams; it is numerically equal to the formula weight in atomic mass units. (Section 3.4)
A compound with the structure R2N!NRO.
An electrically neutral particle found in the nucleus of an atom; it has approximately the same mass as a proton. (Section 2.3)
The product formed when either d-ribose or 2-deoxy-d-ribose is coupled with certain nitrogen heterocycles (called bases).
A constant of proportionality between the reaction rate and the concentrations of reactants that appear in the rate law. (Section 14.3)
The gain of electrons. Alternatively, either the gain of hydrogen, loss of oxygen, or both
The conversion of a ketone or aldehyde into an imine under conditions in which the imine is reduced as soon as it is formed, giving an amine.
Groups that strongy deactivate an aromatic ring toward electrophilic aromatic substitution, thereby significantly decreasing the rate of the reaction.
Two objects that are identical.
A reaction that obeys conservation of orbital symmetry.
Compounds containing a mercapto group (SH).