Nursing Elites

1. Which of the following is the weakest intermolecular force?

• A. Dipole interactions
• B. Hydrogen bonding
• C. Van der Waals forces
• D. Dispersion forces

Correct answer: D

Rationale: Dispersion forces, also known as London dispersion forces, are the weakest intermolecular forces. They are temporary attractive forces that occur due to momentary shifts in electron distribution within molecules. While dipole interactions, hydrogen bonding, and Van der Waals forces are stronger intermolecular forces, dispersion forces are the weakest because they arise from short-lived fluctuations in electron density. Dipole interactions involve permanent dipoles in molecules, making them stronger than dispersion forces. Hydrogen bonding is stronger than dipole interactions and involves hydrogen atoms bonded to highly electronegative atoms. Van der Waals forces encompass dipole-dipole interactions and dispersion forces, making them stronger than dispersion forces alone.

2. What is the name of the force that holds ionic compounds together?

• A. Covalent bonds
• B. Ionic bonds
• C. Hydrogen bonds
• D. Metallic bonds

Correct answer: B

Rationale: Ionic bonds are the forces that hold ionic compounds together. In ionic compounds, positively and negatively charged ions are held together by electrostatic forces of attraction, forming a stable structure. Covalent bonds involve the sharing of electrons between atoms, not the transfer of electrons like in ionic bonds. Hydrogen bonds are a type of intermolecular force, not the primary force in holding ionic compounds together. Metallic bonds are found in metals and involve a 'sea of electrons' that hold metal atoms together, different from the electrostatic attraction between ions in ionic compounds.

3. What color does phenolphthalein turn in the presence of an acid?

• A. Clear
• B. Blue
• C. Pink
• D. Red

Correct answer: C

Rationale: In the presence of an acid, phenolphthalein turns pink. Phenolphthalein is a pH indicator that is colorless in acidic solutions but turns pink in basic solutions. Therefore, when added to an acidic solution, phenolphthalein will exhibit a pink coloration. Choice A, 'Clear,' is incorrect because phenolphthalein does not remain colorless in the presence of an acid. Choice B, 'Blue,' is incorrect as phenolphthalein does not turn blue in the presence of an acid. Choice D, 'Red,' is incorrect as phenolphthalein does not exhibit a red color in acidic solutions.

4. Which two functional groups would you expect an amino acid to contain?

• A. R-NH2 and R-COOH
• B. R-CHO and R-CO-NH
• C. R-OH and R-COOR
• D. R-O-R and R-COOH

Correct answer: A

Rationale: Amino acids are organic compounds that are characterized by the presence of an amino group (NH2) and a carboxylic acid group (COOH) in their chemical structure. These two functional groups, found in option A, are fundamental components of amino acids and play crucial roles in their classification and biological functions. Option B contains an aldehyde group (CHO) and an amide group (CO-NH), which are not characteristic functional groups of amino acids. Option C includes a hydroxyl group (OH) and an ester group (COOR), which are not typically present in amino acids. Option D presents ether (R-O-R) and carboxylic acid (COOH) functional groups, which do not represent the functional groups commonly found in amino acids.

5. What is the oxidation state of the sulfur atom in sulfuric acid H2SO4?

• A. 4
• B. 6
• C. 8
• D. 10

Correct answer: B

Rationale: In sulfuric acid (H2SO4), sulfur has an oxidation state of +6. The oxidation state is determined by considering the overall charge of the compound and the known oxidation states of other elements. In this case, hydrogen is typically +1, and oxygen is -2. To balance the charges and match the compound's overall charge of 0, sulfur must have an oxidation state of +6. Choice A (4) is incorrect because it doesn't balance the charges in the compound. Choices C (8) and D (10) are also incorrect as they are not valid oxidation states for sulfur in this compound.

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