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Solutions for Chapter 4.9: How Specific Rotation Is Measured

Organic Chemistry | 7th Edition | ISBN: 9780321803221 | Authors: Paula Yurkanis Bruice

Full solutions for Organic Chemistry | 7th Edition

ISBN: 9780321803221

Organic Chemistry | 7th Edition | ISBN: 9780321803221 | Authors: Paula Yurkanis Bruice

Solutions for Chapter 4.9: How Specific Rotation Is Measured

Solutions for Chapter 4.9
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This expansive textbook survival guide covers the following chapters and their solutions. This textbook survival guide was created for the textbook: Organic Chemistry, edition: 7. Since 2 problems in chapter 4.9: How Specific Rotation Is Measured have been answered, more than 19106 students have viewed full step-by-step solutions from this chapter. Chapter 4.9: How Specific Rotation Is Measured includes 2 full step-by-step solutions. Organic Chemistry was written by and is associated to the ISBN: 9780321803221.

Key Chemistry Terms and definitions covered in this textbook
  • addition polymers

    Polymers that are formed via cationic addition, anionic addition, or free-radical addition.

  • axial position

    For chair conformations of substituted cyclohexanes, a position that is parallel to a vertical axis passing through the center of the ring.

  • Claisen rearrangement

    A [3,3] sigmatropic rearrangement that is observed for allylic vinylic ethers.

  • deoxyribonucleic acid (DNA)

    A polynucleotide in which the sugar component is deoxyribose. (Section 24.10)

  • enolate

    The resonance-stabilized conjugate base of a ketone, aldehyde, or ester.

  • epimer

    Diastereomers that differ from each other in the configuration of only one chirality center.

  • fission

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

  • Fourier-transform NMR (FT-NMR)

    In nuclear magnetic resonance (NMR) spectroscopy, a technique in which the sample is irradiated with a short pulse that covers the entire range of relevant rf frequencies.

  • Histone

    A protein, particularly rich in the basic amino acids lysine and arginine, that is found associated with DNA molecules

  • hydrohalogenation

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

  • hydronium ion 1H3O+2

    The predominant form of the proton in aqueous solution. (Section 16.2)

  • ionizing radiation

    Radiation that has sufficient energy to remove an electron from a molecule, thereby ionizing it. (Section 21.9)

  • mass number

    The sum of the number of protons and neutrons in the nucleus of a particular atom. (Section 2.3)

  • node

    Points in an atom at which the electron density is zero. For example, the node in a 2s orbital is a spherical surface. (Section 6.6)

  • optical isomerism

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

  • Potential energy

    The energy that can be released if given an opportunity

  • Rate determining step

    The step in a multistep reaction sequence that crosses the highest energy barrier.

  • sp3 Hybrid orbital

    A hybrid atomic orbital formed by the combination of one s atomic orbital and three 2p atomic orbitals.

  • sulfonation

    An electrophilic aromatic substitution reaction in which an SO3H group is installed on an aromatic ring.

  • Trans

    A prefi x meaning across from.

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