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Textbooks / Chemistry / Chemistry: The Central Science 12

Chemistry: The Central Science 12th Edition - Solutions by Chapter

Chemistry: The Central Science | 12th Edition | ISBN: 9780321696724 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward

Full solutions for Chemistry: The Central Science | 12th Edition

ISBN: 9780321696724

Chemistry: The Central Science | 12th Edition | ISBN: 9780321696724 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward

Chemistry: The Central Science | 12th Edition - Solutions by Chapter

Solutions by Chapter
4 5 0 335 Reviews
Textbook: Chemistry: The Central Science
Edition: 12
Author: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward
ISBN: 9780321696724

This expansive textbook survival guide covers the following chapters: 49. Chemistry: The Central Science was written by and is associated to the ISBN: 9780321696724. Since problems from 49 chapters in Chemistry: The Central Science have been answered, more than 173279 students have viewed full step-by-step answer. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 12. The full step-by-step solution to problem in Chemistry: The Central Science were answered by , our top Chemistry solution expert on 04/03/17, 07:58AM.

Key Chemistry Terms and definitions covered in this textbook
  • Acylation

    The process of introducing an acyl group, RCO! or ArCO!, onto an organic molecule.

  • Alditol

    The product formed when the C"O group of a monosaccharide is reduced to a CHOH group.

  • aromatic

    A compound containing a planar ring of continuously overlapping p orbitals with 4n+2p electrons.

  • Bonding molecular orbital

    A molecular orbital in which electrons have a lower energy than they would in isolated atomic orbitals

  • closed system.

    A system that enables the exchange of energy (usually in the form of heat) but not mass with its surroundings. (6.2)

  • decomposition reaction

    A chemical reaction in which a single compound reacts to give two or more products. (Section 3.2)

  • diastereotopic

    Nonequivalent protons for which the replacement test produces diastereomers.

  • Double-headed arrow

    A symbol used to show that structures on either side of it are resonance-contributing structures

  • lactone

    A cyclic ester.

  • Methylene

    A !CH2! group.

  • molality

    The concentration of a solution expressed as moles of solute per kilogram of solvent; abbreviated m. (Section 13.4)

  • nitrogen rule

    In mass spectrometry, an odd molecular weight indicates an odd number of nitrogen atoms in the compound, while an even molecular weight indicates either an even number of nitrogen atoms or the absence of nitrogen.

  • particle accelerator

    A device that uses strong magnetic and electrostatic fields to accelerate charged particles. (Section 21.3)

  • Polar covalent bond

    A covalent bond between atoms whose difference in electronegativity is between approximately 0.5 and 1.9.

  • Polarimeter

    An instrument for measuring the ability of a compound to rotate the plane of plane-polarized light.

  • Radical

    Any chemical species that contains one or more unpaired electrons.

  • Stereospecific reaction

    A special type of stereoselective reaction in which the stereochemistry of the product is dependent on the stereochemistry of the starting material.

  • triglyceride

    A triester formed from glycerol and three long-chain carboxylic acids.

  • vibrational excitation

    In IR spectroscopy, the energy of a photon is absorbed and temporarily stored as vibrational energy

  • Wohl degradation

    A process that involves the removal of a carbon atom from an aldose. The aldehyde group is first converted to a cyanohydrin, followed by loss of HCN in the presence of a base.

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