🥼organic chemistry review

key term - Strong Base

Definition

A strong base is a type of chemical compound that completely dissociates into its constituent ions in an aqueous solution, resulting in a high concentration of hydroxide ions (OH-) and a high pH. Strong bases are important in various organic chemistry reactions, such as the preparation of alkynes via elimination reactions and the Wittig reaction involving phosphorus ylides.

5 Must Know Facts For Your Next Test

  1. Strong bases, such as sodium hydroxide (NaOH) and potassium hydroxide (KOH), are commonly used in organic chemistry reactions to remove a proton (H+) from a substrate, resulting in the formation of a nucleophilic species.
  2. In the preparation of alkynes via the elimination of dihalides, a strong base is used to remove a hydrogen atom and a halogen atom, leading to the formation of a carbon-carbon triple bond.
  3. In the Wittig reaction, a strong base is used to generate a phosphorus ylide, a highly reactive nucleophilic species, which then reacts with a carbonyl compound to form an alkene.
  4. The high pH and high concentration of hydroxide ions in a strong base solution make it a powerful nucleophile and proton acceptor, which is essential for the successful completion of various organic chemistry reactions.
  5. The choice of a strong base in organic chemistry reactions is crucial, as it can influence the reaction's selectivity, rate, and overall outcome.

Review Questions

  • Explain the role of a strong base in the preparation of alkynes via the elimination of dihalides.
    • In the preparation of alkynes from dihalides, a strong base, such as sodium hydroxide (NaOH) or potassium hydroxide (KOH), is used to remove a hydrogen atom and a halogen atom from the dihalide substrate. This elimination reaction results in the formation of a carbon-carbon triple bond, creating the desired alkyne product. The strong base acts as a nucleophile, accepting a proton and facilitating the removal of the halogen, which is a key step in the overall transformation.
  • Describe the role of a strong base in the Wittig reaction, a nucleophilic addition reaction involving phosphorus ylides.
    • In the Wittig reaction, a strong base is used to generate a phosphorus ylide, a highly reactive nucleophilic species, from a phosphonium salt precursor. The strong base, such as n-butyllithium (n-BuLi) or sodium hydride (NaH), deprotonates the phosphonium salt, forming the ylide. This ylide then reacts with a carbonyl compound (aldehyde or ketone) to form an alkene product. The strong base plays a crucial role in activating the phosphorus compound and enabling the nucleophilic addition to the carbonyl, which is a key step in the Wittig reaction mechanism.
  • Analyze the importance of the high pH and high concentration of hydroxide ions (OH-) in a strong base solution for its use in organic chemistry reactions.
    • The high pH and high concentration of hydroxide ions (OH-) in a strong base solution are essential for its use in various organic chemistry reactions. The hydroxide ion is a powerful nucleophile and proton acceptor, which allows it to effectively remove protons (H+) from substrates, generating reactive nucleophilic species. This property is crucial in reactions like the preparation of alkynes via elimination of dihalides and the Wittig reaction involving phosphorus ylides. The high pH of a strong base solution also influences the reaction's selectivity, rate, and overall outcome, making the choice of a strong base a critical factor in the successful completion of these organic transformations.