Exam 3: Acids and Bases

Determine if H₂O is a suitable reagent to protonate the following compound.

For the following reaction, identify the Lewis base.

Predict the products for the following acid-base reaction.

Determine if CH₃CH₂ONa is a suitable reagent to deprotonate the following compound. Explain why. Draw the complete reaction, including the curved arrow mechanism.

For the following reaction identify the acid and the base and predict the products. Draw the curved arrow mechanism for the formation of products and predict the direction of the equilibrium.

Determine if NaOH is a suitable reagent to deprotonate the following compound. Explain why.

For the following reaction, identify the Lewis acid and the Lewis base.

For the following acid-base reaction, predict which side the equilibrium is favored. Explain why.

Which of the following compounds is most acidic?

Which of the following compounds is more acidic? Explain why.

What is the conjugate base of CH₃CH₂SH?

For the following reaction label the acid, base, conjugate acid and conjugate base.

Provide a curved arrow mechanism for the following acid-base reaction.

Rank the indicated protons in decreasing order (most to least) of acidity.

Which of the following compounds is more acidic? Explain why. HF and HBr

Predict the product(s) for the following reaction and draw the curved arrow mechanism.

For the following acid-base reaction, predict which side the equilibrium is favored.

For the following reaction label the acid, base, conjugate acid and conjugate base.

For the following reaction, identify the Lewis base.

In a Brønsted-Lowry acid-base reaction the product(s) is (are) a _______.