Exam 2: Polar Covalent Bonds; Acids and Bases
Exam 1: Structure and Bonding29 Questions
Exam 2: Polar Covalent Bonds; Acids and Bases41 Questions
Exam 3: Organic Compounds: Alkanes and Their Stereochemistry32 Questions
Exam 4: Organic Compounds: Cycloalkanes and Their Stereochemistry29 Questions
Exam 5: Stereochemistry at Tetrahedral Centers40 Questions
Exam 6: An Overview of Organic Reactions39 Questions
Exam 7: Alkenes and Alkynes36 Questions
Exam 8: Reactions of Alkenes and Alkynes38 Questions
Exam 9: Aromatic Compounds37 Questions
Exam 10: Structure Determination: Mass Spectrometry, Infrared Spectroscopy, and Ultraviolet Spectroscopy42 Questions
Exam 10: Structure Determination: Mass Spectrometry, Infrared Spectroscopy, and Ultraviolet Spectroscopy43 Questions
Exam 11: Structure Determination: Nuclear Magnetic Resonance Spectroscopy41 Questions
Exam 12: Organohalides: Nucleophilic Substitutions and Eliminations43 Questions
Exam 13: Alcohols, Phenols, and Thiols; Ethers and Sulfides38 Questions
Exam 14: Aldehydes and Ketones: Nucleophilic Addition Reactions36 Questions
Exam 15: Carboxylic Acids and Nitriles36 Questions
Exam 16: Carboxylic Acid Derivatives: Nucleophilic Acyl Substitution Reactions46 Questions
Exam 17: Carbonyl Alpha-Substitution and Condensation Reactions46 Questions
Exam 18: Amines and Heterocycles36 Questions
Exam 19: Biomolecules: Amino Acids, Peptides, and Proteins52 Questions
Exam 20: Amino Acid Metabolism32 Questions
Exam 21: Biomolecules: Carbohydrates49 Questions
Exam 22: Carbohydrate Metabolism45 Questions
Exam 23: Biomolecules: Lipids and Their Metabolism42 Questions
Exam 24: Biomolecules: Nucleic Acids and Their Metabolism34 Questions
Exam 26: Orbitals and Organic Chemistry: Pericyclic Reactionse44 Questions
Exam 27: Synthetic Polymerse35 Questions
Select questions type
Guanidine is a fairly strong amine base that is attached to the amino acid arginine. Draw three resonance forms for the conjugate acid of guanidine.
guanidine

Free
(Essay)
4.8/5
(39)
Correct Answer:
Which of the following molecules has a dipole moment?
Free
(Multiple Choice)
4.8/5
(41)
Correct Answer:
B
Refer to the following equation to answer the question(s) below.
-Refer to instructions. Will this reaction take place as written in the forward direction? Explain.

Free
(Essay)
4.9/5
(39)
Correct Answer:
No, the reaction will not take place as written because the strongest acid reacts with the strongest base to give the weakest conjugate acid and the weakest conjugate base. D (pKa = 15.7) is a stronger acid than A (pKa = 18).
Complete this acid-base reaction, and label the acid, base, conjugate base, and conjugate acid. 

(Essay)
4.8/5
(34)
Use the convention δ−/δ+ and the crossed arrow (
) to show the direction of the expected polarity of the indicated bonds in the following compound(s).
-Refer to instructions. The C−F bond in fluorobenzene, 


(Essay)
4.8/5
(48)
Use the curved arrow method to show the electron movement, and label the acid, base, conjugate acid, and conjugate base. 

(Essay)
5.0/5
(40)
Refer to the following equation to answer the question(s) below.
-Refer to instructions. The strongest Brønsted-Lowry acid in the equation is indicated by letter _____.

(Multiple Choice)
4.7/5
(40)
Refer to the following equation to answer the question(s) below.
-Refer to instructions. The strongest Brønsted-Lowry base in the equation is indicated by letter _____.

(Multiple Choice)
4.8/5
(39)
Identify the reactants and product in the reaction below as acids or bases and specify whether they are Lewis and/or Brønsted-Lowry.




(Essay)
4.9/5
(37)
Rank the following in order of decreasing importance as a contributing resonance structure to the molecular structure of acetone, CH3COCH3 (more important > less important). A
B
C 



(Multiple Choice)
4.7/5
(35)
Indole is pleasant smelling in highly dilute solutions and has been used in perfumery. Use the structure of indole, below, to answer the following question(s).
-Refer to instructions. Indole can function as a Lewis base in the presence of strong acid. Formulate a reaction, using a generic acid (HA), showing electron flow with arrows, that demonstrates this reactivity of indole.

(Essay)
4.9/5
(37)
Draw a Lewis structure for each of the following.
a)hydroxylammonium ion: +NH3OH.
b)azide ion: (N3−)
(Essay)
4.9/5
(37)
The condensed structure for dimethyl ether looks symmetrical. However, dimethyl ether has a dipole moment. Draw a structure that explains this and indicate the expected direction of the molecular dipole moment.
dimethyl ether

(Essay)
4.8/5
(28)
Which of the following molecules would exhibit the largest dipole moment?
(Multiple Choice)
4.8/5
(38)
In aromatic nitration reactions, nitric acid (HNO3) is used in conjunction with the stronger acid, sulfuric acid, H2SO4, to form an intermediate. Which of the following could be the formula for this intermediate?
(Multiple Choice)
5.0/5
(33)
The visual pigment in animal cells consists of an isomer of retinal linked to the protein opsin, as shown below. Write an alternative resonance form for this species that shows the positive charge situated on the starred carbon instead of the nitrogen atom and include the curved arrows to show the electron flow. 

(Essay)
4.9/5
(39)
Showing 1 - 20 of 41
Filters
- Essay(0)
- Multiple Choice(0)
- Short Answer(0)
- True False(0)
- Matching(0)