1. Factors affecting resonance stability: Structures with complete octets are more stable. Negative charges on more electronegative atoms are favored. Separation of charges decreases stability.
2. Analysis of the given structures: Structure C has significant charge separation and is the least stable. Structure D has localized charges but disrupts the aromatic system, so it is less stable than A and B. Structure A is more stable than C and D because it retains partial resonance. Structure B is the most stable because it has complete resonance and no significant charge separation.
Thus, the correct order of stability is: \[ \text{C} < \text{D} < \text{A} < \text{B}. \]
Identify the products R and S in the reaction sequence given.
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-