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Solutions for Chapter 2.1SE: Chemistry: The Central Science 13th Edition

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown

Full solutions for Chemistry: The Central Science | 13th Edition

ISBN: 9780321910417

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown

Solutions for Chapter 2.1SE

Solutions for Chapter 2.1SE
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Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. Chapter 2.1SE includes 2 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Since 2 problems in chapter 2.1SE have been answered, more than 67668 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • actual yield.

    The amount of product actually obtained in a reaction. (3.10)

  • chromophore

    In UV-Vis spectroscopy, the region of the molecule responsible for the absorption (the conjugated p system).

  • compound

    A substance composed of two or more elements united chemically in definite proportions. (Section 1.2)

  • condensation reaction.

    A reaction in which two smaller molecules combine to form a larger molecule. Water is invariably one of the products of such a reaction. (24.4)

  • electrolytic cell

    A device in which a nonspontaneous oxidation–reduction reaction is caused to occur by passage of current under a sufficient external electrical potential. (Section 20.9)

  • furanose

    A five-membered cyclic hemiacetal form of a carbohydrate.

  • heterogeneous catalyst

    A catalyst that is in a different phase from that of the reactant substances. (Section 14.7)

  • hydration

    Solvation when the solvent is water. (Section 13.1)

  • Hydroperoxide

    A compound containing an !OOH group.

  • Isotactic polymer

    A polymer with identical confi gurations (either all R or all S) at all chiral centers along its chain, as, for example, isotactic polypropylene

  • molecular orbital (MO)

    An allowed state for an electron in a molecule. According to molecular-orbital theory, a molecular orbital is entirely analogous to an atomic orbital, which is an allowed state for an electron in an atom. Most bonding molecular orbitals can be classified as s or p, depending on the disposition of electron density with respect to the internuclear axis. (Section 9.7)

  • phenolate

    The conjugate base of phenol or a substituted phenol.

  • Phospholipid

    A lipid containing glycerol esterifi ed with two molecules of fatty acid and one molecule of phosphoric acid.

  • polydentate ligand

    A ligand in which two or more donor atoms can coordinate to the same metal ion. (Section 23.3)

  • quaternary structure

    The structure of a protein resulting from the clustering of several individual protein chains into a final specific shape. (Section 24.7)

  • redox (oxidation–reduction) reaction

    A reaction in which certain atoms undergo changes in oxidation states. The substance increasing in oxidation state is oxidized; the substance decreasing in oxidation state is reduced. (Section 4.4; Chapter 20: Introduction)

  • reductive amination

    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.

  • SN1 reaction

    A unimolecular nucleophilic substitution reaction.

  • substituents

    In nomenclature, the groups connected to the parent chain.

  • trivalent

    An element, such as nitrogen, that forms three bonds.

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