Question

Thanks in advance!

1. Is hydroxide a strong enough base to deprotonate acetylene in good yield? Explain your answer using a balanced chemical equation with equilibrium arrows. 2. Ozonolysis of 2-hexyne gives two organic products. Name these products 3. Draw the structure of the organic product NaC H DMSO Na (see 10.6) NH3 На Lindlar Pd ОН 4. Draw the keto isomer of the following enol:

Answer 1

No, NaOH cannot take the acetylene proton because the pka of acetylene is 25 in comparison to H20 which is 16. NAOH HC CH OH ОН hex-2-yne NaC Na, NH3() Ну, Pd/C Keto isomer