- 126.96.36.199: Write the structures of all the alkenes that can be formed by dehyd...
- 188.8.131.52: Write structural formulas for all the alkenes that can be formed in...
Solutions for Chapter 5.14: Dehydrohalogenation of Alkyl Halides
Full solutions for Organic Chemistry, | 9th Edition
A reaction in which a reagent adds to the two carbon atoms of a carbon–carbon multiple bond. (Section 24.3)
The conjugate base of a terminal alkyne.
The slow oxidation of organic compounds that occurs in the presence of atmospheric oxygen.
A step in a chain reaction characterized by the formation of reactive intermediates (radicals, anions, or cations) from nonradical or noncharged molecules
A tetrahedral carbon atom bearing four different groups.
A compound containing a Cl group and a hydroxyl group (OH) on adjacent carbon atoms.
A reaction in which two or more substances combine to form a single product. (4.4)
Any three-dimensional arrangement of atoms in a molecule that results from rotation about a single bond.
A compound inwhich two carbon-carbon p bonds are separated from each other by exactly one s bond.
An amorphous solid formed by fusion of SiO2, CaO, and Na2O. Other oxides may also be used to form glasses with differing characteristics. (Section 22.10)
The less substituted product (alkene) of an elimination reaction.
A method for building a peptide from protected building blocks.
nematic liquid crystalline phase
A liquid crystal in which the molecules are aligned in the same general direction, along their long axes, but in which the ends of the molecules are not aligned. (Section 11.7)
A drawing style that is designed to show the conformation of a molecule.
A reaction that takes place in a single step, without intermediates, and involves a cyclic redistribution of bonding electrons
The sequence of amino acids along a protein chain. (Section 24.7)
A chemical entity with an unpaired electron.
The stabilization associated with the delocalization of electrons via resonance.
High-molecular-weight esters that are constructed from carboxylic acids and alcohols.
Williamson ether synthesis
A method for preparing an ether from an alkoxide ion and an alkyl halide (via an SN2 process).
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