di-tert butyl ether cannot be made by Williamson's synthesis. why
Aniline is more basic than p-nitroaniline because the presence of a nitro group (-NO2) in p-nitroaniline decreases its basicity by withdrawing electron density from the amino group. Aniline, on the other hand, lacks this electron-withdrawing group, making it more basic.
Strength of bases is related to the ease of accepting a proton which inturn depends on the availability of electron pair on the nitrogen atom (or some other basic atom). More is the availability of electron pair, more easily the proton will be accepted and more will be the basic strength.Aniline is a weaker base than ammonia or cyclohexylamine. It is because of the fact that the electron pair on nitrogen is involved in delocalization, making it less available for donation.
Pyridine is more basic than aniline primarily due to the presence of the nitrogen atom in a sp² hybridized aromatic ring in pyridine, which allows it to donate its lone pair of electrons more effectively. In contrast, aniline's nitrogen is part of an amine group attached to a benzene ring, where the lone pair is partially delocalized into the aromatic system, making it less available for protonation. This delocalization in aniline reduces its basicity compared to the more localized lone pair on the nitrogen in pyridine.
Aniline is less basic than ammonia because the nitrogen lone pair on aniline is partially delocalized into the benzene ring, making it less available to accept a proton. Ammonia, on the other hand, has a more localized lone pair on nitrogen, which is more readily available for protonation.
Because the electron withdrawing resonance efect caused by the nitro group on the structure, it makes the electrons pair on the nitrogen less available, if the electron pair is less available it's less basic
Yes aniline is heavier than water.Answer:Aniline i slightly denser than water. An equal volume of aniline will have about 2% more mass than water.
Because in Benzylamine : the unshared lone pair of electron on nitrogen atom isavailable >.. But in n-ethyl aniline: the unshared lone pair of electron is not available and enter resonance with benzene ring .(Villa)
Alkyl groups are slightly electron donating. The methyl groups on the amine in N,N dimethylaniline contribute electron density to the nitrogen lone pair, making it more likely to reach out and grab a proton (ie more basic).
Cyclohexylamine is a stronger base than aniline because the nitrogen atom in cyclohexylamine is less hindered by bulky substituents than in aniline. This allows for easier access of the lone pair of electrons on nitrogen in cyclohexylamine, making it more available for proton transfer. Aniline's lone pair is more delocalized into the benzene ring, which reduces its basicity.
Aniline is a stronger base than o-nitroaniline because the nitro group in o-nitroaniline is electron-withdrawing and decreases its basicity compared to aniline. In basicity trends for amines and anilines, the presence of electron-withdrawing groups decreases basicity.
Anilinium chloride is more soluble in water than aniline. This is because anilinium chloride is a salt that dissociates into ions in water, making it more likely to interact with water molecules through ion-dipole interactions. On the other hand, aniline is a neutral molecule that can only interact with water through weaker dipole-dipole interactions.
Since tha pka of the aniline ion is equal to 4.6, the anilinium ion is a stronger acid than the methylaminium ion, and aniline (c6h5nh2) is a weaker base than methylamine (ch3nh2).