The ozonolysis of 2,4,4-trimethyl-2-pentene produces a combination of

and

Explanation: In ozonolysis (where a reducing agent like Zn is involved during hydrolysis), a pi bond cleaves to generate ketones or aldehydes.
Ketones arise from the double bond's disubstituted side, whereas aldehydes come from the monosubstituted side of the same bond.
Notably, ozonolysis comprises two steps: (1) the formation of an ozonide, followed by (2) the hydrolysis of the ozonide.
Hydrolysis can transpire with or without a reducing agent. When it occurs without a reducing agent, carboxylic acid, carbon dioxide, or ketones can be produced.
In this case, 2,4,4-trimethyl-2-pentene yields a mixture of
and 
The reaction process is illustrated below.