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Chemistry: The Central Science 13th Edition - Solutions by Chapter

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

Chemistry: The Central Science | 13th Edition - Solutions by Chapter

Solutions by Chapter
4 5 0 337 Reviews
Textbook: Chemistry: The Central Science
Edition: 13
Author: Theodore E. Brown
ISBN: 9780321910417

This expansive textbook survival guide covers the following chapters: 305. The full step-by-step solution to problem in Chemistry: The Central Science were answered by Sieva Kozinsky, our top Chemistry solution expert on 09/04/17, 02:30PM. Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Since problems from 305 chapters in Chemistry: The Central Science have been answered, more than 59217 students have viewed full step-by-step answer.

Key Chemistry Terms and definitions covered in this textbook
  • Allylic

    Next to a carbon-carbon double bond.

  • anode.

    The electrode at which oxidation occurs. (18.2)

  • antibonding MO

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

  • Beer’s law

    The light absorbed by a substance (A) equals the product of its extinction coefficient 1e2, the path length through which the light passes (b), and the molar concentration of the substance (c): A = ebc. (Section 14.2)

  • benzylic position

    A carbon atom that is immediately adjacent to a benzene ring.

  • Boyle’s law.

    The volume of a fixed amount of gas maintained at constant temperature is inversely proportional to the gas pressure. (5.3)

  • coordination compound.

    A neutral species containing one or more complex ions. (23.3)

  • disulfide bridge

    The group that is formed when two cysteine residues of a polypeptide or protein are joined together.

  • Double helix

    A type of secondary structure of DNA molecules in which two anti parallel polynucleotide strands are coiled in a right-handed manner about the same axis

  • fats

    Triglycerides that are solids atroom temperature.

  • Glycoside

    A carbohydrate in which the !OH on its anomeric carbon is replaced by !OR

  • isoelectric point (pI)

    For an amino acid, the specific pH at which the concentration of the zwitterionic form reaches its maximum value.

  • kinetics

    A term that refers to the rate of a reaction.

  • localized lone pair

    A lone pair thatis not participating in resonance.

  • Mutarotation

    The change in specifi c rotation that occurs when an a or b hemiacetal form of a carbohydrate in aqueous solution is converted to an equilibrium mixture of the two forms.

  • Part per million (ppm)

    Units used on NMR spectra to record chemical shift relative to the TMS standard.

  • Pericyclic reaction

    A reaction that takes place in a single step, without intermediates, and involves a cyclic redistribution of bonding electrons

  • Tautomers

    Constitutional isomers in equilibrium with each other that differ in the location of a hydrogen atom and a double bond relative to a heteroatom, most commonly O, N, or S.

  • tertiary structure

    The threedimensional shape of a protein.

  • Wave function

    A solution to a set of equations that defi nes the energy of an electron in an atom and the region of space it may occupy.

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