Solutions for Chapter 4.8SE: 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 4.8SE

Solutions for Chapter 4.8SE
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Since 2 problems in chapter 4.8SE have been answered, more than 146033 students have viewed full step-by-step solutions from this chapter. Chapter 4.8SE includes 2 full step-by-step solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. This expansive textbook survival guide covers the following chapters and their solutions. Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417.

Key Chemistry Terms and definitions covered in this textbook
  • activated complex (transition state)

    The particular arrangement of atoms found at the top of the potential-energy barrier as a reaction proceeds from reactants to products. (Section 14.5)

  • Allyl

    A !CH2CH"CH2 group.

  • Anomers

    Carbohydrates that differ in confi guration only at their anomeric carbons.

  • beta (b) anomer

    The cyclic hemiacetal of an aldose, in which the hydroxyl group at the anomeric position is cis to the CH2OH group.

  • calorimetry

    The experimental measurement of heat produced in chemical and physical processes. (Section 5.5)

  • chemical kinetics

    The area of chemistry concerned with the speeds, or rates, at which chemical reactions occur. (Chapter 14: Introduction)

  • chlorohydrin

    A compound containing a Cl group and a hydroxyl group (OH) on adjacent carbon atoms.

  • Conjugation

    A situation in which two multiple bonds are separated by a single bond. Alternatively, a series of overlapping 2p orbitals. 1,3-butadiene, for example, is a conjugated diene, and 3-butene-2-one is a conjugated enone

  • covalent bond

    A bond formed between two or more atoms by a sharing of electrons. (Section 8.1)

  • deactivate

    For a substitutedaromatic ring, the effect of an electronwithdrawingsubstituent that decreases therate of electrophilic aromatic substitution.

  • dipole

    A molecule with one end having a partial negative charge and the other end having a partial positive charge; a polar molecule. (Section 8.4)

  • dipole moment

    A measure of the separation and magnitude of the positive and negative charges in polar molecules. (Section 8.4)

  • Ether

    A compound containing an oxygen atom bonded to two carbon atoms.

  • fossil fuels

    Coal, oil, and natural gas, which are presently our major sources of energy. (Section 5.8)

  • law of constant composition

    A law that states that the elemental composition of a pure compound is always the same, regardless of its source; also called the law of definite proportions. (Section 1.2)

  • matter waves

    The term used to describe the wave characteristics of a moving particle. (Section 6.4)

  • nucleophilic aromatic substitution

    A substitution reaction in which an aromatic ring is attacked by a nucleophile, which replaces a leaving group.

  • Reductive elimination

    Elimination of two substituents at a metal center, causing the oxidation state of the metal to decrease by two.

  • Sharpless asymmetric epoxidation

    A reaction that converts an alkene into an epoxide via a stereospecific pathway.

  • vinylic carbocation

    A carbocation in which the positive charge resides on a vinylic carbon atom. This type of carbocation is very unstable and will not readily form in most cases.

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