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Why acetanilide brominates in the ortho and para positions and the amount of o-bromoacetanilide?
Acetanilide undergoes bromination in the ortho and para positions due to the presence of the activating amino group that directs the electrophilic bromine to these positions. In the reaction mixture, the para-bromoacetanilide is the major product compared to the ortho isomer, typically in a ratio of about 4:1.
What is the end product of nitro benzene is nitrated at 125 degree Celsius with mixed acids?
The end product of nitrobenzene being nitrated at 125 degrees Celsius with mixed acids would be a mixture of meta-nitrobenzene (major product) and ortho-nitrobenzene (minor product). The reaction conditions favor the formation of the meta isomer due to the lower activation energy for the meta position.
Why does para-chlorophenol melts at 43 degrees Celsius and ortho-chlorophenol melts at 9 degrees Celsius?
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Why is anisole ortho and para director towards electrophile substitution reaction?
Anisole is ortho and para directing in electrophilic aromatic substitution reactions because the lone pairs on the oxygen atom can donate electron density to the ring through resonance, stabilizing the carbocation intermediate formed during the reaction at the ortho and para positions. This makes those positions more favorable for electrophilic attack.
Which is more acidic orthohydroxybenzoic acid or metahydroxybenzoic acid?
Orthohydroxybenzoic acid is more acidic than metahydroxybenzoic acid because the hydroxy group is in closer proximity to the carboxylic acid group in the ortho position, allowing for a stronger intramolecular hydrogen bond and greater stability of the conjugate base.
Why acetanilide brominates in the ortho and para positions and the amount of o-bromoacetanilide?
Acetanilide undergoes bromination in the ortho and para positions due to the presence of the activating amino group that directs the electrophilic bromine to these positions. In the reaction mixture, the para-bromoacetanilide is the major product compared to the ortho isomer, typically in a ratio of about 4:1.
What is the end product of nitro benzene is nitrated at 125 degree Celsius with mixed acids?
The end product of nitrobenzene being nitrated at 125 degrees Celsius with mixed acids would be a mixture of meta-nitrobenzene (major product) and ortho-nitrobenzene (minor product). The reaction conditions favor the formation of the meta isomer due to the lower activation energy for the meta position.
What is the reaction of phenol with Bromine?
The hydroxyl group in phenol is an activating ortho/para director, but has some slight steric hindrance too ortho position substitution. Therefore, the predominant product of reaction between phenol and bromine will be 4-bromophenol, if reaction conditions are carefully controlled. With excess bromine, di- and tri-bromo phenols will be formed.
What is the major product(s) of the monochlorination of fluorobenzene?
The major product of the monochlorination of fluorobenzene is chlorofluorobenzene. Due to the electron-withdrawing effect of the fluorine atom, chlorination tends to occur at the ortho and para positions relative to the fluorine, with the para product often being favored due to steric factors. However, since fluorine is a powerful deactivator, the overall reaction rate is slower compared to chlorobenzene.
The major product obtained on interaction of phenol with sodium hydroxide and carbon dioxide is?
The major product obtained from the interaction of phenol with sodium hydroxide and carbon dioxide is sodium phenoxide. This is formed through the reaction between phenol and sodium hydroxide to give sodium phenolate, which further reacts with carbon dioxide to form sodium phenoxide and water.
How can you produce parabromobenzealdehyde from bromobenzene?
When a mixture of carbonmonoxide and HCl is added to Bromobenzene (Gatterman's reaction) a mixture of ortho and para product is obtained which may be separated on the bases of solubilities.
Why is o-bromoacetanilide is removed from p-isomer?
O-bromoacetanilide is removed from the p-isomer due to the differences in polarity and solubility between the isomers during purification processes, such as recrystallization or chromatography. The p-isomer, which has the bromo group in the para position, is generally more stable and less polar than the o-isomer, allowing for easier separation based on these physical properties. Additionally, the steric hindrance and electronic effects in the ortho position can lead to different reactivity, facilitating the removal of the o-isomer.
Can you have an allergic reaction to Ortho-tricyclen lo?
Yes, you can. See the Related Link.
What are lipid types other than unsaturated?
The two types are saturated and unsaturated. In the unsaturated there are two subtypes: monounsaturated and polyunsaturated. There are five isomer types: cis-, trans-, ortho-, meta-, and para-
Why does para-chlorophenol melts at 43 degrees Celsius and ortho-chlorophenol melts at 9 degrees Celsius?
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Why is anisole ortho and para director towards electrophile substitution reaction?
Anisole is ortho and para directing in electrophilic aromatic substitution reactions because the lone pairs on the oxygen atom can donate electron density to the ring through resonance, stabilizing the carbocation intermediate formed during the reaction at the ortho and para positions. This makes those positions more favorable for electrophilic attack.
What brand of birth control pills have ortho tricyclen?
Ortho Tricyclen is made by Ortho.
