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What is the major product of reaction of 4-Ethyl methoxy benzene in the presence of chlorine and AlCl3?
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∙ 14y ago
The major product is 2-chloro-4-ethyl methoxybenzene.
Wiki User
∙ 14y ago
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Which functional group is present in structure of haloperidol?
alkane haloalkane amide alcohol ketone not so much a functional group but it does contain ring structures like benzene
Bromocyclopentane plus methoxy what product?
Bromocyclopentane and methoxy makes chloride. This is made from raw materials.
Which is more acidic ortho-nitro benzoic acid or ortho-methoxy benzoic acid?
orho methoxy benzoic acid is more acidic due to stability achieved due to chelation effect.
What is the IUPAC name of ohcch2ch2coch2cooh?
that is methyl propyl ether. aka methoxy propane. not methoxy propyl ether. methyl propyl ether has 1 oxygen. methoxy propyl ether has 2 oxygens.
12-ethyl-3-methoxy-gona-diene 17 6-17 dihydroxyetiocholove-3-ol propionate?
Havoc Clone? definitely not a havoc clone. havoc is methylated and is epistane. this is a progestin, similar to 13-ethyl (max-lmg) with a few structural differences. also, these are two separate compounds. 12-ethyl-3-methoxy-gona-diene is a prohormone while the rest is an aromatase inhibitor.
Which functional group is present in structure of haloperidol?
alkane haloalkane amide alcohol ketone not so much a functional group but it does contain ring structures like benzene
Melting point of methyl methoxy?
The melting point of methyl methoxy is -113 degrees Celsius. The boiling point of methyl methoxy is 7.4 degrees Celsius.
Bromocyclopentane plus methoxy what product?
Bromocyclopentane and methoxy makes chloride. This is made from raw materials.
What is the structural formula of methoxy ethane?
Ch3och2ch3
What is the use of Methoxy propanol?
It is a solvent used for production of paints.
Which is more acidic ortho-nitro benzoic acid or ortho-methoxy benzoic acid?
orho methoxy benzoic acid is more acidic due to stability achieved due to chelation effect.
What is an anisole?
An anisole is a type of aromatic compound that has a methoxy group (-OCH3) attached to a benzene ring. It is often used as a solvent in various chemical reactions and as a starting material for the synthesis of other compounds. Anisole has a sweet, pleasant odor and is a colorless liquid at room temperature.
What is the IUPAC name of ohcch2ch2coch2cooh?
that is methyl propyl ether. aka methoxy propane. not methoxy propyl ether. methyl propyl ether has 1 oxygen. methoxy propyl ether has 2 oxygens.
What is the ortho-peradirective nature?
I think you're asking about ortho-para directors. o,p directors are groups bonded to a benzene ring that direct additional groups in electrophilic aromatic substitution reactions to attach to the ortho and para positions of the benzene ring. Ortho is the position next to the group and para is the position across from the group on the benzene ring. o,p directors are electron donating groups such as methoxy groups. These groups stabilize the positive charge created in the intermediate when the electrophile adds to the ortho and para positions. o,p directors do not, however, stabilize the positive charge when the electrophile adds to the meta position and therefore only allow addition to the ortho and para positions (thus the name ortho-para director).
What ethyl alcohol solution has 3-methoxy 4-hydroxy benzaldehyde?
You think probable to vanillin essence.
Why does the reaction of 2 2-dimethyloxirane with sodium methoxide in methanol gives primarily 1-methoxy-2-methyl-2-propanol?
Methoxide is your nucleophile; it will attack the C3 of 2,2-dimethyloxirane (the carbon that is attached to the oxygen, but doesn't have any methyl groups) via backside attack. This will cause the bond between C3 and the oxygen to break, thus releasing the chain and forming the oxide form of 1-methoxy-2-methyl-2-propanol. Since the oxide of this product is more basic than methanol, it will rip the hydrogen off of methanol, which will create the final product and regenerate methoxide.
What is dimethoxyaniline?
It's aniline with two methoxy substituents; I don't think it has a common name. It's used in the manufacture of aniline dyes and pigments.
