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Solutions for Chapter 3.2SE: Chemistry: A Molecular Approach 3rd Edition

Chemistry: A Molecular Approach | 3rd Edition | ISBN: 9780321809247 | Authors: Nivaldo J. Tro

Full solutions for Chemistry: A Molecular Approach | 3rd Edition

ISBN: 9780321809247

Chemistry: A Molecular Approach | 3rd Edition | ISBN: 9780321809247 | Authors: Nivaldo J. Tro

Solutions for Chapter 3.2SE

Solutions for Chapter 3.2SE
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Chemistry: A Molecular Approach was written by and is associated to the ISBN: 9780321809247. Since 2 problems in chapter 3.2SE have been answered, more than 433609 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Chemistry: A Molecular Approach, edition: 3. This expansive textbook survival guide covers the following chapters and their solutions. Chapter 3.2SE includes 2 full step-by-step solutions.

Key Chemistry Terms and definitions covered in this textbook
  • adhesion.

    Attraction between unlike molecules. (11.3)

  • Aldehyde

    A compound containing a !CHO group

  • alkaline earth metals.

    The Group 2A elements (Be, Mg, Ca, Sr, Ba, and Ra). (2.4)

  • anti-coplanar

    A conformation in which a hydrogen atom and a leaving group are separated by a dihedral angle of exactly 180°.

  • becquerel

    The SI unit of radioactivity. It corresponds to one nuclear disintegration per second. (Section 21.4)

  • bending

    In IR spectroscopy, a type of vibration that generally produces a signal in the fingerprint region of an IR spectrum.

  • Bond length

    The distance between atoms in a covalent bond in picometers (pm; 1 pm 5 10212 m) or Å (1Å 5 10210 m).

  • bonding MO

    A low-energy molecular orbital resulting from the constructive interference between atomic orbitals.

  • bonding pair

    In a Lewis structure a pair of electrons that is shared by two atoms. (Section 9.2)

  • chromophore

    In UV-Vis spectroscopy, the region of the molecule responsible for the absorption (the conjugated p system).

  • combination reaction.

    A reaction in which two or more substances combine to form a single product. (4.4)

  • configuration

    The 3D spatial orientation of the groups connected to a chirality center (R or S ) or of the groups in a stereoisiomeric alkene (E or Z).

  • Coupling constant

    The separation on an NMR spectrum (in hertz) between adjacent peaks in a multiplet and a quantitative measure of the infl uence of the spin-spin coupling with adjacent nuclei.

  • exo

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

  • internal alkyne

    A compound with the structure R!C#C!R, where each R group is not a hydrogen atom.

  • nucleophilic acyl substitution

    A reaction in which a nucleophile attacks a carboxylic acid derivative.

  • phenoxide

    The conjugate base of phenol or a substituted phenol.

  • radiotracer

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

  • rate-determining step

    The sloweststep in a multistep reaction which determines the rate of the reaction.

  • reductive amination

    The conversion of a ketone or aldehyde into an imine under conditions in which the imine is reduced as soon as it is formed, giving an amine.

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