1-Propanol shows the normal reaction befitting a primary alcohol. Therefore can be converted to alkyl halides; for example red phosphorus and iodium produce n-propyl iodide with 80% yield, while PCl3 with catalytic ZnCl2 produce with 1-kloropropana. Reaction with acetic acid in the presence of H2SO4 catalyst under Fischer eseterifikasi produce propyl acetate. While refluxing propanol for one night with formic acid produce propyl format deNGAN 65% yield. Oxidation of 1-propanol with Na2Cr2O7 and H2SO4 generates propionaldehida with only 36% yield, and therefore for this type of reaction is recommended using PCC or the swern Oxidations to increase yield. Oxidation with chromic acid yields propionic acid 1-Propanol shows the normal reaction befitting a primary alcohol. Therefore can be converted to alkyl halides; for example red phosphorus and iodium produce n-propyl iodide with rendemen 80%, while PCl3 with catalytic ZnCl2 produce with 1-kloropropana. Reaction with acetic acid in the presence of H2SO4 catalyst under Fischer eseterifikasi produce propyl acetate. While refluxing propanol for one night with formic acid produce propyl format with a 65% yield. Oxidation of 1-propanol with Na2Cr2O7 and H2SO4 generates propionaldehida with only 36% yield, and therefore for this type of reaction is recommended using PCC or oxy
