Nitration of aniline in strong acidic medium

Question Description Why nitration of aniline in strong acidic medium also gives m- nitroaniline .solv this que with easy solutn.? for NEET 2023 is part of NEET preparation. The Question and answers have been prepared according to the NEET exam syllabus. Information about Why nitration of aniline in strong acidic medium also gives m- nitroaniline .solv this que with easy solutn.? covers all topics & solutions for NEET 2023 Exam. Find important definitions, questions, meanings, examples, exercises and tests below for Why nitration of aniline in strong acidic medium also gives m- nitroaniline .solv this que with easy solutn.?. Here you can find the meaning of Why nitration of aniline in strong acidic medium also gives m- nitroaniline .solv this que with easy solutn.? defined & explained in the simplest way possible. Besides giving the explanation of Why nitration of aniline in strong acidic medium also gives m- nitroaniline .solv this que with easy solutn.?, a detailed solution for Why nitration of aniline in strong acidic medium also gives m- nitroaniline .solv this que with easy solutn.? has been provided alongside types of Why nitration of aniline in strong acidic medium also gives m- nitroaniline .solv this que with easy solutn.? theory, EduRev gives you an ample number of questions to practice Why nitration of aniline in strong acidic medium also gives m- nitroaniline .solv this que with easy solutn.? tests, examples and also practice NEET tests.

• A first-order reaction can catalyzed; a second-order reaction cannot be catalyzed • The half-life of a first-order reaction does not depend on [ A ] 0 ​ ; the half-life of a second-order reaction does depend on [ A ] 0 ​ • The rate of a first-order reaction does not depend on reactant concentrations; the rate of a second-order reaction does depend on reactant concentrations • The rate of a first-order reaction does depend on reactant concentrations; the rate of a second-order reaction does not depend on reactant concentrations

People Also Read: Corect option is C) Nitration of aniline in strong acidic medium also gives m-nitroaniline because in acidic (strong) medium aniline is present as anilinium ion. Amino −NH 2 group is ortho-para directing but −NH 3+ group is meta directing. When the nitration of aniline is done in the strong acidic medium it gives m- nitroaniline because in strong medium the aniline is present as the anilinium ion. as we know that the nitro [N] group is a strong electron withdrawing group so it will go towards that atom which has more electron density. What is Nitration of aniline in strong acidic medium also gives m nitroaniline On nitration of aniline with concentrated acids, a good amount of meta nitro aniline is obtained. Although the amino group is 0- and p-directing in aromatic electrophilic substitution reactions, aniline on nitration gives a substantial amount of nitroaniline. Nitration of aniline in a strongly acidic medium gives a mixture of o-nitroaniline, p-nitroaniline, and m- nitroaniline. Aniline is having -NH2 group on the benzene ring. How to use Nitration of aniline in the strong acidic medium also gives $m It is a volatile substance used as a raw material in production of dyes. It is stable in neutral, basic as well as acidic medium. Nitration of aniline in strong acidic medium also gives m -nitroaniline because (a) inspite of. ) medium aniline is present as anilinium ion. Following solutions were prepared by mixing different volumes of N aOH and H Cl of...

Nitration of aniline in the strong acidic medium also gives m- nitroaniline because _______A) In absence of substituents nitro group always goes to m- positionsB) In spite of substituents nitro group always goes to only m- positionsC) In strong acidic medium aniline is present as anilinium ionD) In electrophilic substitution reactions aminos group is meta directive Nitration of aniline in the strong acidic medium also gives m- nitroaniline because _______ A) In absence of substituents nitro group always goes to m- positions B) In spite of substituents nitro group always goes to only m- positions C) In strong acidic medium aniline is present as anilinium ion D) In electrophilic substitution reactions aminos group is meta directive Hint: Aniline is a yellow colour compound which has a brownish shade oily liquid having musty and fishy odour. The smell of aniline is just like a rotten fish. It is a flammable liquid. It is soluble in water and even freely soluble in chemicals such as ether and alcohol. It gets dark in colour when it is exposed to air and light. Complete step-by-step answer: It is toxic in nature when someone inhales it through air or when it gets absorbed in skin as it tends to produce nitrogen oxides which are harmful. When the nitration of aniline is done in the strong acidic medium it gives m- nitroaniline because in strong medium the aniline is present as the anilinium ion.as we know that the nitro \[Nm-nitroaniline\] So the correct answer is option ‘C’. No...

Nitration of aniline in strong acidic medium also gives m -nitroaniline because (a) inspite of substituents nitro group always goes to only m-position (b) in electrophilic substitution reactions amino group is meta directive (c) in absence of substituents nitro group always goes to m-position (d) in acidic (strong) medium aniline is present as anilinium ion. Correct option (d) in acidic (strong) medium aniline is present as anilinium ion. Explanation : The reason for the formation of an unexpected amount of m-nitroaniline is that under a strongly acidic condition of nitration, most of the aniline is converted into anilinium ion and since. is a m -directing group, therefore, a large amount of m-nitroaniline is also obtained.