The most stable carbocation is (c). The stability of the carbocation is enhanced by the +M (mesomeric) effect of the \( \text{NH}_2 \) group, which donates electron density into the ring, stabilizing the positive charge on the carbocation. In this case, the resonance structures show that the positive charge is delocalized, making this carbocation the most stable.
Thus, the correct answer is:C
Number of \( ^1H \) NMR signals observed for the following compound is .............
The product(s) in the following transformation is(are)
The major products P and Q of the following reactions are
The major product in the following reaction sequence is
Pericyclic reactions involved in the synthesis of Vitamin D\(_2\) from Ergosterol are
Let one focus of the hyperbola $ \frac{x^2}{a^2} - \frac{y^2}{b^2} = 1 $ be at $ (\sqrt{10}, 0) $, and the corresponding directrix be $ x = \frac{\sqrt{10}}{2} $. If $ e $ and $ l $ are the eccentricity and the latus rectum respectively, then $ 9(e^2 + l) $ is equal to:
The largest $ n \in \mathbb{N} $ such that $ 3^n $ divides 50! is:
Organic Chemistry is a subset of chemistry dealing with compounds of carbon. Therefore, we can say that Organic chemistry is the chemistry of carbon compounds and is 200-225 years old. Carbon forms bond with itself to form long chains of hydrocarbons, e.g.CH4, methane and CH3-CH3 ethane. Carbon has the ability to form carbon-carbon bonds quite elaborately. Polymers like polyethylene is a linear chain where hundreds of CH2 are linked together.
Read Also: Organic Compounds
Organic chemistry is applicable in a variety of areas including-