Exam 1: Structure and Bonding
Exam 1: Structure and Bonding127 Questions
Exam 2: Acids and Bases; Functional Groups136 Questions
Exam 3: Structure and Stereochemistry of Alkanes134 Questions
Exam 4: The Study of Chemical Reactions128 Questions
Exam 5: Stereochemistry132 Questions
Exam 6: Alkyl Halides; Nucleophilic Substitution137 Questions
Exam 7: Structure and Synthesis of Alkenes; Elimination131 Questions
Exam 8: Reactions of Alkenes134 Questions
Exam 10: Structure and Synthesis of Alcohols136 Questions
Exam 11: Reactions of Alcohols125 Questions
Exam 12: Infrared Spectroscopy and Mass Spectrometry121 Questions
Exam 13: Nuclear Magnetic Resonance Spectroscopy130 Questions
Exam 14: Ethers, Epoxides, and Thioethers127 Questions
Exam 15: Conjugated Systems, Orbital Symmetry, and Ultraviolet Spectroscopy130 Questions
Exam 16: Aromatic Compounds128 Questions
Exam 17: Reactions of Aromatic Compounds129 Questions
Exam 18: Ketones and Aldehydes131 Questions
Exam 19: Amines127 Questions
Exam 20: Carboxylic Acids125 Questions
Exam 21: Carboxylic Acid Derivatives130 Questions
Exam 22: Condensations and Alpha Substitutions of Carboxyl Compounds127 Questions
Exam 23: Carbohydrates and Nucleic Acids126 Questions
Exam 24: Amino Acids, Peptides, and Proteins127 Questions
Exam 25: Lipids127 Questions
Exam 26: Synthetic Polymers128 Questions
Select questions type
Calculate the empirical and molecular formulas of the compound with molecular weight 122 and an elemental analysis of 59.01% C, 4.97% H, 13.12% O, and 22.90% N.
(Essay)
4.8/5
(44)
Nitroamines are common functional groups found in energetic materials, such as RDX and HMX. For the structure below, draw two other significant resonance structures, include any formal charges, and indicate the hybridization on each nitrogen and oxygen. 

(Essay)
4.8/5
(30)
In the following acid/base reaction, label the acid, base, conjugate acid and conjugate base.
NH3 + H- → NH2- + H2
(Essay)
4.8/5
(42)
In the reaction below, label each reactant as a nucleophile or an electrophile.
CH3COO- + O2S(OCH3)2 → CH3COOCH3 + CH3OSO3-
(Essay)
4.8/5
(49)
One or more of the atoms in the structure shown should have nonzero formal charges. Redraw the structure and the atoms with non-zero formal charges. 

(Essay)
4.8/5
(35)
Strong bases usually contain positively charged atoms of high electronegativity and no resonance stabilization.
(True/False)
4.8/5
(45)
Within a given row of the periodic table, electronegativity typically increases left to right across the row.
(True/False)
5.0/5
(42)
How many distinct p orbitals exist in the second electron shell, where n = 2?
(Multiple Choice)
4.9/5
(36)
What is the molecular formula for the following line-angle structure? 

(Short Answer)
4.7/5
(39)
One or more of the atoms in the structure shown should have nonzero formal charges. Add the correct formal charge/s. (All non-bonding electrons have been included.) 

(Essay)
4.8/5
(39)
For most compounds in which a nitrogen atom bears no formal charge, the valence of this nitrogen atom is ________.
(Short Answer)
4.9/5
(33)
Which of the following pairs of bases lists the stronger base first?
(Multiple Choice)
4.8/5
(30)
Which sequence correctly ranks the following protons in order of increasing pKa value? 

(Multiple Choice)
4.7/5
(45)
The Lewis structure of pentane is shown below. Draw the condensed structural formula which corresponds to this Lewis structure. 

(Essay)
4.7/5
(35)
Draw a correct Lewis structure for tert-butyl alcohol, (CH3)3COH, including all non-bonding lone pairs.
(Essay)
4.7/5
(39)
Write a Lewis structure for a compound with the molecular formula H2N2.
(Essay)
4.9/5
(35)
The electron density of ________ orbitals has spherical symmetry.
(Short Answer)
4.9/5
(42)
A condensed structure for acetone is CH3COCH3. Provide the structural formula for acetone.
(Essay)
4.8/5
(36)
Showing 41 - 60 of 127
Filters
- Essay(0)
- Multiple Choice(0)
- Short Answer(0)
- True False(0)
- Matching(0)