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An isomeric form of propyl is obtained by moving the point of attachment from a terminal carbon atom to the central carbon atom, named isopropyl or 1-methylethyl. To maintain four substituents on each carbon atom, one hydrogen atom has to be moved from the middle carbon atom to the carbon atom which served as attachment point in the n -propyl ...
Propyl propanoate (also known as propyl propionate and n-propyl propionate) is the organic compound with the molecular formula C 6 H 12 O 2. It is the ester of propanol and propionic acid. Like most esters, propyl propanoate is a colorless liquid with a fruity odor. The scent of propyl propionate is described as a chemically tinged pineapple or ...
(CH 3) 2 CHCH 2 COOH 2-methylbutanoic acid: 2-methylbutiric acid: CH 3 CH 2 CH(CH 3)COOH 2,2-dimethylpropanoic acid: pivalic acid trimethylacetic acid neopentanoic acid (CH 3) 3 CCOOH 3-hydroxypentanoic acid: β-hydroxyvaleric acid 3-hydroxyvaleric acid β-hydroxypentanoate: CH 3 CH 2 CHOHCH 2 COOH 4-hydroxypentanoic acid: γ-hydroxyvaleric ...
If the alkyl group is not attached at the end of the chain, the bond position to the ester group is suffixed before "-yl": CH 3 CH 2 CH(CH 3)OOCCH 2 CH 3 may be called butan-2-yl propanoate or butan-2-yl propionate. [citation needed]. The prefix form is "oxycarbonyl-" with the (R') group preceding.
1-Propanol, n-propanol, or propan-1-ol: CH 3 CH 2 CH 2 OH, the most common meaning 2-Propanol, isopropyl alcohol , isopropanol, or propan-2-ol: (CH 3 ) 2 CHOH See also
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Isopropyl chloride is an organic compound with the chemical formula (CH 3) 2 CHCl. It is a colourless to slightly yellow, volatile, flammable liquid with a sweet, ether-like (almost like petroleum) odour. It is used as an industrial solvent. It is produced industrially by the addition of HCl to propylene: [1] CH 3 CH=CH 2 + HCl → (CH 3) 2 CHCl
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