- 1.7SE.1PE: Determining the Number of Significant Figures in a MeasurementHow m...
- 1.7SE.2PE: Determining the Number of Significant Figures in a MeasurementHow m...
Solutions for Chapter 1.7SE: Chemistry: The Central Science 13th Edition
Full solutions for Chemistry: The Central Science | 13th Edition
ISBN: 9780321910417
Chemistry: The Central Science was written by and is associated to the ISBN: 9780321910417. Chapter 1.7SE includes 2 full step-by-step solutions. This expansive textbook survival guide covers the following chapters and their solutions. Since 2 problems in chapter 1.7SE have been answered, more than 309886 students have viewed full step-by-step solutions from this chapter. This textbook survival guide was created for the textbook: Chemistry: The Central Science, edition: 13.
-
1,4-addition
A reaction involving the addition of two groups to a conjugated p system in which one group is installed at the C1 position and the other group is installed at the C4 position.
-
amide
An organic compound that has an NR2 group attached to a carbonyl. (Section 24.4)
-
antiaromatic
Instability that arises when a planar ring of continuously overlapping p orbitals contains 4n p electrons.
-
biodegradable polymers
Polymers that can be broken down by enzymes produced by soil microorganisms.
-
boiling-point elevation (DTb).
The boiling point of the solution (Tb) minus the boiling point of the pure solvent (T° b). (12.6)
-
carboxylic acid
A compound that contains the ¬COOH functional group. (Sections 16.10 and 24.4)
-
cell voltage.
Difference in electrical potential between the anode and the cathode of a galvanic cell. (18.2)
-
Chromatography
A separation method involving passing a vapor or solution mixture through a column packed with a material with different affi nities for different components of the mixture.
-
conjugate addition
An addition reaction in which a nucleophile and a proton are added across the two ends of a conjugated p system.
-
Conjugate addition
Addition of a nucleophile to the b-carbon of an a,b-unsaturated carbonyl compound. (Section 20.2A) Addition to carbons 1 and 4 of a conjugated diene.
-
cycloalkanes.
Alkanes whose carbon atoms are joined in rings. (24.2)
-
Equatorial bond
A bond to a chair conformation of cyclohexane that extends from the ring roughly perpendicular to the imaginary axis through the center of the ring; a bond that lies roughly along the equator of a cyclohexane ring
-
London dispersion forces
Attractive forces between transient dipole moments, observed in alkanes.
-
oxaphosphetane
An intermediate that is believed to be formed during Wittig reactions.
-
primary cell
A voltaic cell that cannot be recharged. (Section 20.7)
-
Raman spectroscopy
A vibrational molecular spectroscopy that is complementary to infrared (IR) spectroscopy in that infrared inactive vibrations are seen in Raman spectroscopy.
-
Resonance hybrid
A molecule, ion, or radical described as a composite of a number of contributing structures
-
Schiff base
An alternative name for an imine
-
SN2 reaction
A bimolecular nucleophilic substitution reaction.
-
unsaturated
A compound containingone or more p bonds.