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Solutions for Chapter 24.1SE: Chemistry: The Central Science 13th Edition

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

Solutions for Chapter 24.1SE

Solutions for Chapter 24.1SE
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This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13. This expansive textbook survival guide covers the following chapters and their solutions. Chemistry: The Central Science was written by Sieva Kozinsky and is associated to the ISBN: 9780321910417. Chapter 24.1SE includes 2 full step-by-step solutions. Since 2 problems in chapter 24.1SE have been answered, more than 67758 students have viewed full step-by-step solutions from this chapter.

Key Chemistry Terms and definitions covered in this textbook
  • acylium ion

    The resonancestabilized, cationic intermediate of a Friedel-Crafts acylation, formed by treating an acyl halide with aluminum trichloride.

  • alcohol

    An organic compound obtained by substituting a hydroxyl group 1¬OH2 for a hydrogen on a hydrocarbon. (Sections 2.9 and 24.4)

  • aldehydes.

    Compounds with a carbonyl functional group and the general formula RCHO, where R is an H atom, an alkyl, or an aromatic group. (24.4)

  • amidomalonate synthesis

    A synthetic method that employs diethyl acetamidomalonate as the starting material and enables the preparation of racemic a-amino acids.

  • Anomeric carbon

    The hemiacetal or acetal carbon of the cyclic form of a carbohydrate

  • boiling-point elevation (DTb).

    The boiling point of the solution (Tb) minus the boiling point of the pure solvent (T° b). (12.6)

  • bonding MO

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

  • Clemmensen reduction

    A reaction in which a carbonyl group is completely reduced and replaced with two hydrogen atoms.

  • conjugate addition

    An addition reaction in which a nucleophile and a proton are added across the two ends of a conjugated p system.

  • cyanides.

    Compounds containing the CN2 ion. (22.3)

  • decomposition reaction

    A chemical reaction in which a single compound reacts to give two or more products. (Section 3.2)

  • 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

  • Line-angle formula

    An abbreviated way to draw structural formulas in which vertices and line endings represent carbons

  • Polyester

    A polymer in which each monomer unit is joined to the next by an ester bond, as, for example, poly(ethylene terephthalate).

  • potential energy

    The energy that an object possesses as a result of its composition or its position with respect to another object. (Section 5.1)

  • sterically hindered

    A compound or region of a compound that is very bulky.

  • sulfoxide

    A compound containing an SRO bond that is flanked on both sides by R groups.

  • thermodynamic control

    A reaction for which the ratio of products is determined solely by the distribution of energy among the products.

  • torsional angle

    The angle between two groups in a Newman projection, also called the dihedral angle.

  • zwitterion

    A net neutral compound that exhibits charge separation. Amino acids exist as zwitterions at physiological pH.

Textbook Survival Guides

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