9-BBN's steric hindrance raises questions about its reactivity with internal alkynes and alkenes for hydroboration. While some sources suggest that 9-BBN can react with internal alkenes, it is anticipated that the reaction rate would be slower compared to terminal alkenes. The design of 9-BBN, featuring larger substituents, aims to promote boron addition at less hindered sites, enhancing regioselectivity. Compared to borane-THF, 9-BBN is noted for its greater regioselectivity, and its availability in solid form offers practical advantages over gaseous B2H6.