Final answer:
The order of increasing nucleophilicity in acetone is CH3OH, CH3SH, CH3NH2.
Step-by-step explanation:
In order to rank the species in order of increasing nucleophilicity in acetone, we need to consider the relative nucleophilic strength of the different species. Nucleophilicity is generally related to the ability of a species to donate an electron pair. Higher nucleophilicity corresponds to a stronger ability to donate electrons. Among the given species, the order of increasing nucleophilicity in acetone would be:
- CH3OH
- CH3SH
- CH3NH2
Step-by-step explanation:
- CH3OH (methanol) is more nucleophilic than CH3SH (methanethiol) because oxygen is more electronegative than sulfur, making the oxygen more willing to donate its electron pair.
- CH3SH is more nucleophilic than CH3NH2 (methylamine) because sulfur is more polarizable than nitrogen, allowing the sulfur to better accommodate an extra electron pair.