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What are the possible isomers of chlorohexane?
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
Why are substitutions at 4' and 6' positions of 3-chloro toluene not normally possible?
Substitutions at 4' and 6' positions of 3-chloro toluene are not normally possible because carbocations are prone to rearrangement.
How do you draw the structure 5-chloro-3-ethyl-4-methyloctane?
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)
Is 4-methylcyclohexanol solubility in hexane?
4-methylcyclohexanol is soluble in hexane because it is a nonpolar molecule, similar to hexane. Nonpolar solutes tend to be soluble in nonpolar solvents like hexane due to similar intermolecular forces.
Molecular formula of hexane?
The molecular formula of all the hexanes is C6H14. (Remember the numbers should be subscripts.) However there are isomers: CH3CH2CH2CH2CH2CH3, (CH 3 ) 2 CH(CH 2 ) 2 CH 3 CH 3 CH 2 CH(CH 3 )CH 2 CH 3 CH 3 CH(CH 3 )CH(CH 3 )CH 3 CH 3 C(CH 3 ) 2 CH 2 CH 3 Wikipedia shows them clearly.
What are the possible isomers of chlorohexane?
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
Does 3-chloro-3-methylhexane have optical isomers?
Yes. 4 different groups are bonded to the third carbon atom.
What are the properties and uses of 1-chloro-4-methyl-benzene?
1-chloro-4-methyl-benzene is a chemical compound with properties that make it useful in various industries. It is a colorless liquid with a strong odor, and it is flammable. This compound is commonly used as a solvent in chemical reactions and as an intermediate in the production of pharmaceuticals and agrochemicals. Additionally, it can be used in the synthesis of dyes, perfumes, and other organic compounds.
How do you write structure of 3-ethyl-4-methylhexane?
C-C-C-C-C-C hexane 3rd C gets a CH2CH3 for ethyl 4th C gets a CH3 for methyl
What is the chemical structure of 1 chloro-4 methyl cyclohexane and what are its properties?
The chemical structure of 1-chloro-4-methylcyclohexane is a cyclohexane ring with a chlorine atom attached to carbon 1 and a methyl group attached to carbon 4. This compound is a colorless liquid with a slightly sweet odor. It is insoluble in water but soluble in organic solvents. It is flammable and may cause irritation to the skin, eyes, and respiratory system upon exposure.
What is the name of the chemical which has 7 carbon atoms and 16 hydrogen atoms?
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.
Why are substitutions at 4' and 6' positions of 3-chloro toluene not normally possible?
Substitutions at 4' and 6' positions of 3-chloro toluene are not normally possible because carbocations are prone to rearrangement.
How do you draw the structure 5-chloro-3-ethyl-4-methyloctane?
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)
What is 4-chloro?
Halodrol
What is the IUPAC name of cresol?
o Cresol 2-methyl phenol m Cresol 3-methyl phenol p- Cresol 4- methyl phenol
Is 4-methylcyclohexanol solubility in hexane?
4-methylcyclohexanol is soluble in hexane because it is a nonpolar molecule, similar to hexane. Nonpolar solutes tend to be soluble in nonpolar solvents like hexane due to similar intermolecular forces.
What is the common name of 4-bromo-3-methylheptanal?
The common name of 4-bromo-3-methylheptanal is Bromo-methyl heptanal.
