- 19.19.27: a. Does a coupling reaction have to be used to synthesize p -diprop...
- 19.19.28: Show how each of the following compounds can be synthesized from be...
Solutions for Chapter 19.19: SYNTHESIS OF MONOSUBSTITUTED AND DISUBSTITUTED BENZENES
Full solutions for Organic Chemistry | 7th Edition
ISBN: 9780321803221
Solutions for Chapter 19.19: SYNTHESIS OF MONOSUBSTITUTED AND DISUBSTITUTED BENZENES
Get Full SolutionsChapter 19.19: SYNTHESIS OF MONOSUBSTITUTED AND DISUBSTITUTED BENZENES includes 2 full step-by-step solutions. Organic Chemistry was written by and is associated to the ISBN: 9780321803221. This expansive textbook survival guide covers the following chapters and their solutions. Since 2 problems in chapter 19.19: SYNTHESIS OF MONOSUBSTITUTED AND DISUBSTITUTED BENZENES have been answered, more than 17166 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7.
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alkyl amines
A format for naming amines containing simple alkyl groups.
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Avogadro’s law
A statement that the volume of a gas maintained at constant temperature and pressure is directly proportional to the number of moles of the gas. (Section 10.3)
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basic oxide (basic anhydride)
An oxide that either reacts with water to form a base or reacts with an acid to form a salt and water. (Section 22.5)
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bond-line structures
The most common drawing style employed by organic chemists. All carbon atoms and most hydrogen atoms are implied but not explicitly drawn in a bond-line structure.
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carbohydrates
A class of substances formed from polyhydroxy aldehydes or ketones. (Section 24.8)
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conjugate acid–base pair
An acid and a base, such as H2O and OH-, that differ only in the presence or absence of a proton. (Section 16.2)
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Cope rearrangement
A [3,3] sigmatropic rearrangement in which all six atoms of the cyclic transition state are carbon atoms.
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Dalton’s law of partial pressures.
The total pressure of a mixture of gases is just the sum of the pressures that each gas would exert if it were present alone. (5.6)
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Edman degradatio
A method for selectively cleaving and identifying the N-terminal amino acid of a polypeptide chain.
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Electron affinity
Energy added or released when an electron is added to an atom or molecule.
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keto-enol tautomerization
The equilibrium that is established between an enol and a ketone in either acid-catalyzed or basecatalyzed conditions.
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Newman projection
A way to view a molecule by looking along a carbon-carbon single bond
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Optically active
Refers to a compound that rotates the plane of plane-polarized light
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oxidizing agent, or oxidant
The substance that is reduced and thereby causes the oxidation of some other substance in an oxidation–reduction reaction. (Section 20.1)
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Pauli exclusion principle
No more than two electrons may be present in an orbital. If two electrons are present, their spins must be paired
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quantitative analysis
The determination of the amount of a given substance that is present in a sample. (Section 17.7)
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quaternary structure
The structure that arises when a protein consists of two or more folded polypeptide chains that aggregate to form one protein complex.
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renewable energy sources
Energy such as solar energy, wind energy, and hydroelectric energy derived from essentially inexhaustible sources. (Section 5.8)
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terminal alkynes
Compounds with the following structure: R!C#C!H
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Thermoplastic
A polymer that can be melted and molded into a shape that is retained when it is cooled.