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Solutions for Chapter 2: Chemistry: The Central Science 12th Edition

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

Solutions for Chapter 2

Solutions for Chapter 2
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Textbook: Chemistry: The Central Science
Edition: 12
Author: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward
ISBN: 9780321696724

Since 122 problems in chapter 2 have been answered, more than 315923 students have viewed full step-by-step solutions from this chapter. Chemistry: The Central Science was written by and is associated to the ISBN: 9780321696724. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 12. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 2 includes 122 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • Aldose

    A monosaccharide containing an aldehyde group

  • antiaromatic

    Instability that arises when a planar ring of continuously overlapping p orbitals contains 4n p electrons.

  • base.

    A substance that yields hydroxide ions (OH2) when dissolved in water. (2.7)

  • cation

    A positively charged ion. (Section 2.7)

  • chemical property.

    Any property of a substance that cannot be studied without converting the substance into some other substance. (1.6)

  • coordination number.

    In a crystal lattice it is defined as the number of atoms (or ions) surrounding an atom (or ion) (11.4). In coordination compounds it is defined as the number of donor atoms surrounding the central metal atom in a complex. (23.3)

  • copolymer

    A complex polymer resulting from the polymerization of two or more chemically different monomers. (Section 12.8)

  • Deshielding

    The term used to express the concept of less shielding in NMR

  • exo

    In Diels-Alder reactions that produce bicyclic structures, the positions that are anti to the larger bridge.

  • Frost circles

    A simple method for drawing the relative energy levels of the MOs for a ring assembled from continuously overlapping p orbitals.

  • glass transition temperature (Tg)

    The temperature at which noncrystalline polymers become very soft.

  • Halohydrin

    A compound containing a halogen atom and a hydroxyl group on adjacent carbons; those containing Br and OH are bromohydrins, and those containing Cl and OH are chlorohydrins.

  • heterogeneous catalyst

    A catalyst that does not dissolve in the reaction medium.

  • Hydration

    The addition of water.

  • limiting reactant (limiting reagent)

    The reactant present in the smallest stoichiometric quantity in a mixture of reactants; the amount of product that can form is limited by the complete consumption of the limiting reactant. (Section 3.7)

  • monosaccharide

    A simple sugar, most commonly containing six carbon atoms. The joining together of monosaccharide units by condensation reactions results in formation of polysaccharides. (Section 24.8)

  • osmotic pressure

    The pressure that must be applied to a solution to stop osmosis from pure solvent into the solution. (Section 13.5)

  • solution alloy

    A homogeneous alloy, where two or more elements are distributed randomly and uniformly throughout the solid. (Section 12.3)

  • Stereospecific reaction

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

  • unsaturated

    A compound containingone or more p bonds.