Solutions for Chapter 7.3SE: 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 7.3SE

Solutions for Chapter 7.3SE
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Since 2 problems in chapter 7.3SE have been answered, more than 146639 students have viewed full step-by-step solutions from this chapter. 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. Chapter 7.3SE includes 2 full step-by-step solutions. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13.

Key Chemistry Terms and definitions covered in this textbook
  • acylium ion

    The resonancestabilized, cationic intermediate of a Friedel-Crafts acylation, formed by treating an acyl halide with aluminum trichloride.

  • Alkyne

    An unsaturated hydrocarbon that contains one or more carbon-carbon triple bonds.

  • boranes

    Covalent hydrides of boron. (Section 22.11)

  • condensation reaction

    A chemical reaction in which a small molecule (such as a molecule of water) is split out from between two reacting molecules. (Sections 12.6 and 22.8)

  • denaturation

    A process during which a protein unfolds under conditions of mild heating.

  • deuterium

    The isotope of hydrogen whose nucleus contains a proton and a neutron: 2 1H. (Section 22.2)

  • d–d transition

    The transition of an electron in a transition-metal compound from a lower-energy d orbital to a higher-energy d orbital. (Section 23.6)

  • endothermic

    Any process with a positive DH (the system receives energy from the surroundings).

  • Fat

    A mixture of triglycerides that is semisolid or solid at room temperature.

  • Fischer projections

    A drawing style that is often used when dealing with compounds bearing multiple chirality centers, especially for carbohydrates. (See also Sect. 5.7.)

  • fission

    The splitting of a large nucleus into two smaller ones. (Section 21.6)

  • heterolytic bond cleavage

    Bond breaking that results in the formation of ions.

  • hydrohalogenation

    A reaction that involves the addition of H and X (either Br or Cl) across an alkene.

  • Kiliani-Fischer synthesis

    A process by which the chain of a carbohydrate is lengthened by one carbon atom.

  • Markovnikov’s rule

    In the addition of HX, H2O, or ROH to an alkene, hydrogen adds to the carbon of the double bond having the greater number of hydrogens.

  • pH

    The negative log in base 10 of the aquated hydrogen ion concentration: pH = -log3H+4. (Section 16.4)

  • phospholipids

    Esterlike derivatives of phosphoric acid.

  • photon

    When electromagnetic radiation is viewed as a particle, an individual packet of energy.

  • Prostaglandin

    A member of the family of compounds having the 20-carbon skeleton of prostanoic acid

  • radiotracer

    A radioisotope that can be used to trace the path of an element in a chemical system. (Section 21.5)

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