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Solutions for Chapter 5.11SE: Chemistry: The Central Science 13th Edition

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

Full solutions for Chemistry: The Central Science | 13th Edition

ISBN: 9780321910417

Chemistry: The Central Science | 13th Edition | ISBN: 9780321910417 | Authors: Theodore E. Brown; H. Eugene LeMay; Bruce E. Bursten; Catherine Murphy; Patrick Woodward; Matthew E. Stoltzfus

Solutions for Chapter 5.11SE

Solutions for Chapter 5.11SE
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This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. Since 2 problems in chapter 5.11SE have been answered, more than 263291 students have viewed full step-by-step solutions from this chapter. Chapter 5.11SE includes 2 full step-by-step solutions. Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417. This expansive textbook survival guide covers the following chapters and their solutions.

Key Chemistry Terms and definitions covered in this textbook
  • aldonic acid

    The product obtained when the aldehyde group of an aldose is oxidized.

  • Alkaloid

    A basic nitrogen-containing compound of plant origin, many of which are physiologically active when administered to humans.

  • alloy

    A substance that has the characteristic properties of a metal and contains more than one element. Often there is one principal metallic component, with other elements present in smaller amounts. Alloys may be homogeneous or heterogeneous. (Section 12.3)

  • coupling (of protons)

    A phenomenon observed most commonly for nonequivalent protons connected to adjacent carbon atoms in which the multiplicity of each signal is affected by the other.

  • Deshielding

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

  • diazotization

    The process of forming a diazonium salt by treating a primary amine with NaNO2 and HCl.

  • E2

    A bimolecular eliminationreaction.eclipsed conformation (Sect. 4.7): A conformationin which groups are eclipsing each other in aNewman projection.

  • electrophile

    A compound containing an electron-deficient atom that is capable of accepting a pair of electrons.

  • Enantiotopic groups

    Atoms or groups on an atom that give a chiral center when one of the groups is replaced by another group. A pair of enantiomers results. The hydrogens of the CH2 group of ethanol, for example, are enantiotopic. Replacing one of them by deuterium gives (R)-1-deuteroethanol; replacing the other gives (S)-1-deuteroethanol. Enantiotopic groups have identical chemical shifts in achiral environments but different chemical shifts in chiral environments.

  • functional group

    A characteristic group of atoms/bonds that possess a predictable chemical behavior.

  • hydride shift

    A type of carbocation rearrangement that involves the migration of a hydride ion (H-).

  • molecular-orbital diagram

    A diagram that shows the energies of molecular orbitals relative to the atomic orbitals from which they are derived; also called an energy-level diagram. (Section 9.7)

  • Monosaccharide

    A carbohydrate that cannot be hydrolyzed to a simpler carbohydrate.

  • 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)

  • 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.

  • Newman projection

    A drawing style that is designed to show the conformation of a molecule.

  • oxidation state

    A method of electron book-keeping in which all bonds are treated as if they were purely ionic.

  • ozonolysis

    A reaction in which the CRC bond of an alkene is cleaved to form two CRO bonds.

  • racemic mixture

    A mixture of equal amounts of the dextrorotatory and levorotatory forms of a chiral molecule. A racemic mixture will not rotate the plane of polarized light. (Section 23.4)

  • Triglyceride (triacylglycerol)

    An ester of glycerol with three fatty acids

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