CH3-CH2-CH(CH3)-CH(Cl)-CH2-CH3
I can only think of 14 of them, but i know there are a few more 1-chlorohexane 2-chlorohexane 3-chlorohexane 1-chloro-2-methylpentane 1-chloro-3-methylpentane 1-chloro-4-methylpentane 2-chloro-3-methylpentane 2-chloro-4-methylpentane 3-chloro-2-methylpentane 1-chloro-2,2-dimethylbutane 3-chloro-2,2-dimethylbutane 1-chloro-3,3-dimethylbutane 1-chloro-2,3-dimethylbutane 2-chloro-2,3-dimethylbutane
Substitutions at 4' and 6' positions of 3-chloro toluene are not normally possible because carbocations are prone to rearrangement.
To begin with, octane is a chain of 8 carbons. If you were to draw these eight carbons in a row and number them 1-8, then the numbers corresponding to the substituents (chloro, ethyl and methyl) will show you where to put them. Off of the fifth carbon from one end (make sure you are consistent with which end you use!) is Cl Off of the third carbon is the ethyl group (CH2-CH3) and off of the fourth is the methyl group (CH3)
yes
This compound is used as derivative of a coccidiostat in poultry farming.It should not be made at home.5-chloro 4-(acetylamino)2-methoxy methylbenzoate2(CH3O-)4(CH3CONH-)-5(Cl-)C6H5COO(CH3) (chemical compound))
I can only think of 14 of them, but i know there are a few more 1-chlorohexane 2-chlorohexane 3-chlorohexane 1-chloro-2-methylpentane 1-chloro-3-methylpentane 1-chloro-4-methylpentane 2-chloro-3-methylpentane 2-chloro-4-methylpentane 3-chloro-2-methylpentane 1-chloro-2,2-dimethylbutane 3-chloro-2,2-dimethylbutane 1-chloro-3,3-dimethylbutane 1-chloro-2,3-dimethylbutane 2-chloro-2,3-dimethylbutane
The simplest one is the ALKANE , Heptane. (C7H16) CH3CH2CH2CH2CH2CH2CH3 It has numerous isomers. 2-methyl-hexane , 3-methyl-hexane, 4-methyl-hexane 3-ethyl-pentane. 1-methlycyclohexane 1-ethylcyclopentane, 1,2-dimethyl-cyclopentane, 1,3-dimethyl-cyclopentane 1,2,3-trimethylcyclobutane, 1-ethyl-2-methylcyclobutane. 1,2,-dimethyl-3-ethyl-cyclopropane, NB The cyclobutanes and cyclopropanes are unstable, because of the strained ring structure.
C-C-C-C-C-C hexane 3rd C gets a CH2CH3 for ethyl 4th C gets a CH3 for methyl
Substitutions at 4' and 6' positions of 3-chloro toluene are not normally possible because carbocations are prone to rearrangement.
To begin with, octane is a chain of 8 carbons. If you were to draw these eight carbons in a row and number them 1-8, then the numbers corresponding to the substituents (chloro, ethyl and methyl) will show you where to put them. Off of the fifth carbon from one end (make sure you are consistent with which end you use!) is Cl Off of the third carbon is the ethyl group (CH2-CH3) and off of the fourth is the methyl group (CH3)
Halodrol
o Cresol 2-methyl phenol m Cresol 3-methyl phenol p- Cresol 4- methyl phenol
Yes. 4 different groups are bonded to the third carbon atom.
14 1-heptyne 2-heptyne 3-heptyne 3-methyl-1-hexyne 4-methyl-1-hexyne 5-methyl-1-hexyne 4-methyl-2-hexyne 5-methyl-2-hexyne 2-methyl-3-hexyne 3,3-dimethyl-1-pentyne 4,4-dimethyl-1-pentyne 3-ethyl-1-pentyne 3,4-dimethyl-1-pentyne 2,2-dimethyl-3-pentyne
yes
The four isomers of the compound dichloropropane are 1,1-dichloropropane, 1,2-dichloropropane, 1,3-dichloropropane and 2,2-dichloropropane. The chemical formula for dichloropropane is C3H6Cl2.
4 methyl (3, 5 dinitro) phenylol