CH3, methyl; ethyl, C2H5; amyl nowadays called pentyl, C5H11.
Methyl
An alkane. Hence the name alkyl. An alkane is a chain of carbon atoms bonded to each other with single bonds, with hydrogen atoms filling the remainder of the bonds. One hydrogen atom is replaced by a halogen to form an alkyl halide.
One electron from the metal is transferred to the halogen to produce a metal halide and an alkyl radical.R-X + M → R• + M+X− The alkyl radical then accepts an electron from another metal atom to form an alkyl anion and the metal becomes cationic. This intermediate has been isolated in a several cases.R• + M → R−M+ The nucleophilic carbon of the alkyl anion then displaces the halide in an SN2 reaction, forming a new carbon-carbon covalent bond.R−M+ + R-X → R-R + M+X−
Alcohol (or ethanol) has a hydroxyl (OH) group on the end of its carbon chain, and contains no double bonds. Alkanes are likewise a single chain of carbon atoms joined by single bonds, but have no -OH group attached to them.
When one hydrogen is removed from an alkane it forms alkyl group
Alcohol is an organic compound that has a hydroxyl functional group bound to a carbon atom. A short-chain alcohol have alkyl chains of one to three carbons.
An alkane. Hence the name alkyl. An alkane is a chain of carbon atoms bonded to each other with single bonds, with hydrogen atoms filling the remainder of the bonds. One hydrogen atom is replaced by a halogen to form an alkyl halide.
halo alkane or alkyl halides
One electron from the metal is transferred to the halogen to produce a metal halide and an alkyl radical.R-X + M → R• + M+X− The alkyl radical then accepts an electron from another metal atom to form an alkyl anion and the metal becomes cationic. This intermediate has been isolated in a several cases.R• + M → R−M+ The nucleophilic carbon of the alkyl anion then displaces the halide in an SN2 reaction, forming a new carbon-carbon covalent bond.R−M+ + R-X → R-R + M+X−
Alcohol (or ethanol) has a hydroxyl (OH) group on the end of its carbon chain, and contains no double bonds. Alkanes are likewise a single chain of carbon atoms joined by single bonds, but have no -OH group attached to them.
R = aryl or alkyl group. O = Oxygen, C = Carbon, H = Hydrogen. With that said: R-COOH Indicates an aryl/alkyl bound to a carbon, bound to two oxygens and one oxygen is bound to a hydrogen. If you complete their valence shells you get. R-C=O | O-H
Alkylation is a chemical process involving carbon atoms. In refineries, this is done to add octane to gasoline by introducing hydrocarbons to the fuel.
When one hydrogen is removed from an alkane it forms alkyl group
Webster's new world dictionary defines ethereal as: adj. 1. very light; airy; delicate 2. not earthly; heavenly
If u are referring to the carbocations of n-butyl, sec-butyl, and t-butyl, the most stable is the one that has the most alkyl groups attached to the positively charged carbon atom. In this case: - n-butyl has only 1 alkyl group attached - sec-butyl has 2 alkyl groups attached - t-butyl has 3 alkyl groups attached Therefore, t-butyl is the most stable carbocation
Alcohol is an organic compound that has a hydroxyl functional group bound to a carbon atom. A short-chain alcohol have alkyl chains of one to three carbons.
An aldehyde contains a portion with the structural formula HC=O, with one additional bond of the carbon atom to hydrogen or carbon.CnH2nOC2h4oRCHO - Where R represents any alkyl group.Please see the link below for a list of aldelhyde chemical formulas.
there will be three peaks. one for the carbons in ferrocene around 70 -75. one for the carbonyl carbon (around 200) and one for the methyl group in acetyl (around alkyl region).