
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.



For the circuit shown above, the equivalent gate is:
Let \( f : \mathbb{R} \to \mathbb{R} \) be a twice differentiable function such that \[ (\sin x \cos y)(f(2x + 2y) - f(2x - 2y)) = (\cos x \sin y)(f(2x + 2y) + f(2x - 2y)), \] for all \( x, y \in \mathbb{R}. \)
If \( f'(0) = \frac{1}{2} \), then the value of \( 24f''\left( \frac{5\pi}{3} \right) \) 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-