- 4.2.4.3: Give the structure for each of the following: (a) 2-methylpropene (...
- 4.2.4.4: Name the following compounds. Ignore double-bond stereochemistry. (...
- 4.2.4.5: Name each of the following compounds, including the proper designat...
- 4.2.4.6: Give the structure of: (a) (E)-4-allyl-1,5-octadiene (b) (2E,7Z)-5-...
- 4.2.4.7: In each case, which group receives the higher priority? (a) (b) (c)...
Solutions for Chapter 4.2: NOmENCLATURE OF ALKENES
Full solutions for Organic Chemistry | 6th Edition
ISBN: 9781936221349
This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 6. Chapter 4.2: NOmENCLATURE OF ALKENES includes 5 full step-by-step solutions. Organic Chemistry was written by and is associated to the ISBN: 9781936221349. Since 5 problems in chapter 4.2: NOmENCLATURE OF ALKENES have been answered, more than 50013 students have viewed full step-by-step solutions from this chapter.
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Activating group
Any substituent on a benzene ring that causes the rate of electrophilic aromatic substitution to be greater than that for benzene.
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adhesion.
Attraction between unlike molecules. (11.3)
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anion.
An ion with a net negative charge. (2.5)
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bond enthalpy.
The enthalpy change required to break a bond in a mole of gaseous molecules. (9.10)
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Carbenoid
A compound that delivers the elements of a carbene without actually producing a free carbene.
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cathodic protection
A means of protecting a metal against corrosion by making it the cathode in a voltaic cell. This can be achieved by attaching a more easily oxidized metal, which serves as an anode, to the metal to be protected. (Section 20.8)
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concentration cell
A voltaic cell containing the same electrolyte and the same electrode materials in both the anode and cathode compartments. The emf of the cell is derived from a difference in the concentrations of the same electrolyte solutions in the compartments. (Section 20.6)
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conformation
A three-dimensional shape that can be adopted by a compound as a result of rotation about single bonds.
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covalent bond.
A bond in which two electrons are shared by two atoms. (9.4)
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eicosanoids
A class of lipids which includes leukotrienes, prostaglandins, thromboxanes, and prostacyclins.
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electromotive force (emf)
A measure of the driving force, or electrical pressure, for the completion of an electrochemical reaction. Electromotive force is measured in volts: 1 V = 1 J>C. Also called the cell potential. (Section 20.4)
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energy
The capacity to do work or to transfer heat. (Section 5.1)
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Faraday constant (F )
The magnitude of charge of one mole of electrons: 96,500 C>mol. (Section 20.5)
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gamma radiation
Energetic electromagnetic radiation emanating from the nucleus of a radioactive atom. (Section 21.1)
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molecular formula
A chemical formula that indicates the actual number of atoms of each element in one molecule of a substance. (Section 2.6)
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neutron
An electrically neutral particle found in the nucleus of an atom; it has approximately the same mass as a proton. (Section 2.3)
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oxime
A compound with the structure R2CRN!OH.
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Phenol
A compound that contains an !OH bonded to a benzene ring; a benzenol.
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Polyamide
A polymer in which each monomer unit is joined to the next by an amide bond, as, for example, nylon 66.
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polyether
A compound containing several ether groups.