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Textbooks > Chemistry > Chemistry: Matter & Change 1

Chemistry: Matter & Change 1st Edition - Solutions by Chapter

Chemistry: Matter & Change | 1st Edition | ISBN: 9780078746376 | Authors: McGraw-Hill Education

Full solutions for Chemistry: Matter & Change | 1st Edition

ISBN: 9780078746376

Chemistry: Matter & Change | 1st Edition | ISBN: 9780078746376 | Authors: McGraw-Hill Education

Chemistry: Matter & Change | 1st Edition - Solutions by Chapter

Since problems from 24 chapters in Chemistry: Matter & Change have been answered, more than 36440 students have viewed full step-by-step answer. Chemistry: Matter & Change was written by and is associated to the ISBN: 9780078746376. This textbook survival guide was created for the textbook: Chemistry: Matter & Change, edition: 1. This expansive textbook survival guide covers the following chapters: 24. The full step-by-step solution to problem in Chemistry: Matter & Change were answered by , our top Chemistry solution expert on 11/10/17, 05:56PM.

Key Chemistry Terms and definitions covered in this textbook
  • allylic carbocation

    A carbocation in which the positive charge is adjacent to a carbon-carbon double bond.

  • alpha (a) helix

    For proteins, a feature of secondary structure that forms when a portion of the protein twists into a spiral.

  • antibonding MO

    A high-energy molecular orbital resulting from the destructive interference between atomic orbitals.

  • Aufbau principle.

    As protons are added one by one to the nucleus to build up the elements, electrons similarly are added to the atomic orbitals. (7.9)

  • Covalent bond

    A chemical bond formed between two atoms by sharing one or more pairs of electrons.

  • elimination (of radicals)

    In radical reaction mechanisms, a step in which a bond forms between the alpha (a) and beta (b) positions. As a result, a single bond at the b position is cleaved, causing the compound to fragment into two pieces.

  • Gauche conformation

    A conformation about a single bond of an alkane in which two groups on adjacent carbons lie at a dihedral angle of 60°

  • Haworth projection

    A way to view furanose and pyranose forms of monosaccharides. The ring is drawn fl at and most commonly viewed through its edge with the anomeric carbon on the right and the oxygen atom of the ring to the rear

  • heat of reaction

    The heat given off during a reaction.

  • Hybridization

    The combination of atomic orbitals of different types

  • lanthanide contraction

    The gradual decrease in atomic and ionic radii with increasing atomic number among the lanthanide elements, atomic numbers 57 through 70. The decrease arises because of a gradual increase in effective nuclear charge through the lanthanide series. (Section 23.1)

  • mercurinium ion

    The intermediateformed during oxymercuration.

  • normal melting point

    The melting point at 1 atm pressure. (Section 11.6)

  • Nucleoside

    A building block of nucleic acids, consisting of d-ribose or 2-deoxy-d-ribose bonded to a heterocyclic aromatic amine base by a b-N-glycosidic bond

  • optical isomerism

    A form of isomerism in which the two forms of a compound (stereoisomers) are nonsuperimposable mirror images. (Section 23.4)

  • optically active

    Possessing the ability to rotate the plane of polarized light. (Section 23.4)

  • polyvinyl chloride, (PVC)

    A polymer formed from the polymerization of vinyl chloride (H2CRCHCl).

  • SN2

    A bimolecular nucleophilic substitution reaction.

  • Transfer RNA (tRNA

    A ribonucleic acid that carries a specifi c amino acid to the site of protein synthesis on ribosomes

  • Woodward-Fieser rules

    Rules for predicting the wavelength of maximum absorption for a compound with extended conjugation.

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