1. Oxidation of secondary alcohols:
\[
R{-}CH(OH){-}R' \xrightarrow{[O]} R{-}C(=O){-}R' + H_2O
\]
2. Ozonolysis of alkenes:
\[
RCH{=}CHR' \xrightarrow[\ ]{O_3/Zn,H_2O} R{-}C(=O){-}R'
\]
3. Friedel–Crafts acylation of aromatic compounds:
\[
C_6H_6 + RCOCl \xrightarrow{AlCl_3} C_6H_5COR + HCl
\]
4. From calcium salts of carboxylic acids (dry distillation):
\[
(COO)_2Ca \;\xrightarrow{\Delta}\; R{-}C(=O){-}R + CaCO_3
\]
5. From nitriles (using dialkyl cadmium):
\[
RCN + R'_{2}Cd \;\longrightarrow\; R{-}C(=O){-}R'
\]
Thus, ketones can be prepared by oxidation, ozonolysis, acylation, dry distillation, and nitrile methods.