Dyes are of several types they may be acidic , basic or neutral, organic dyes are mostly basic.
Aniline is a stronger base than o-nitroaniline.
acid, or LSD is a psychedelic drug that can make you trip balls. LSD dose not have any relation to any sort of aniline or base.
It's is weak base!
Acetanilide is not an acid nor a base.
Aniline is polar.
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POLar
No, all isomers of this formula are neutral alcohols not the base.
Aniline is a base and forms salt with HCl which is soluble in water.
aniline is weaker base because it is stabilized by resonance leaving less negative charge to hold the proton.
aniline and benzaldehyde combines to form a C6H5N=CHH5C6 type of imine
Aniline doesnt undergo friedel craft rxn because the reagent AlCl3,(the lewis acid which is used as a catalyst in friedel crafts reaction).being e- deficient acts as lewis base and attacks on the lone pair of nitrogen present in aniline & aniline forms a salt with Aluminium chloride. Due to this nitrogen atom of aniline acquires a positive charge and hence acts as a strong deactivating group and thus doesn 't allow the reaction to take place.In other cases ther is no such reaction.
No, all isomers of this formula are neutral alcohols not the base.
Aniline is a base and forms salt with HCl which is soluble in water.
aniline is weaker base because it is stabilized by resonance leaving less negative charge to hold the proton.
aniline and benzaldehyde combines to form a C6H5N=CHH5C6 type of imine
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).
aniline would go through an electrophilic substitution, it is a weak base
Aniline doesnt undergo friedel craft rxn because the reagent AlCl3,(the lewis acid which is used as a catalyst in friedel crafts reaction).being e- deficient acts as lewis base and attacks on the lone pair of nitrogen present in aniline & aniline forms a salt with Aluminium chloride. Due to this nitrogen atom of aniline acquires a positive charge and hence acts as a strong deactivating group and thus doesn 't allow the reaction to take place.In other cases ther is no such reaction.
The lone pair on the nitrogen of aniline is delocalised into the pi-system of the benzene ring and is therefore less available for attack on a proton.
in the case of aniline, the lone pair on nitrogen is involved in resonance with the benzene ring, hence its basicity decreases. no such resonance is seen in cyclohexyl amine, and the lone pair is available to abstract protons and it is stronger base than aniline.
There is no any such difference between Aniline point and mixed Aniline point . . . . .
It is a strong base.
There is likely no reaction, aniline is a base that upon aquiring a proton converts to a stable ammonium cation, ferric nitrate( Fe(NO3)2 ) has no protons to donate to the amine group of aniline means it will likely not react. In addition the nitrate ion of ferric nitrate is the conjugate base of Nitric acid and is thus extremely stable isn't likely to react with much of anything.