NaNH2 is too strong a base to do a dehydrohalogenation of a geminal dihalide.Select answer from the options belowTrueFalse

Analysis of the Statement

1. Understanding the Context

   • In chemistry, dehydrohalogenation is the elimination of hydrogen halides from a dihalide compound to form a double bond.
   • Geminal dihalides have two halogen atoms attached to the same carbon atom.

2. Reactivity of NaNH2

   • Sodium amide (NaNH2) is a strong base and is often used in dehydrohalogenation reactions.
   • However, the reactivity of a strong base can lead to competing reactions, especially with certain substrates.

3. Geminal Dihalides and Reaction Conditions

   • Geminal dihalides are more prone to elimination reactions because they can lead to the formation of alkenes.
   • The strong basicity of NaNH2 might lead to other side reactions or could be too reactive for controlled elimination.

Verification of the Statement

• Strong bases like NaNH2 may indeed be considered "too strong" for selective dehydrohalogenation of geminal dihalides due to their reactivity leading to unwanted side reactions.

Final Conclusion

True: NaNH2 is too strong a base to effectively perform a controlled dehydrohalogenation of a geminal dihalide.