A methyl group attached to a carbocation stabilizes it through hyperconjugation. Hyper-conjugation involves the interaction of the electrons in the C-H sigma bonds of the methyl group with the empty p-orbital of the positively charged carbon. This delocalization of electron density stabilizes the carbocation.
Match the Compounds (List - I) with the appropriate Catalyst/Reagents (List - II) for their reduction into corresponding amines. 
Consider the following amino acid: 
Which of the following options contain the correct structure of (A) and (B)?
