![product [A], [B], and [C] in the following reaction](https://images.collegedunia.com/public/qa/images/content/2025_03_17/Screenshot_029098311742200193386.jpeg)
![product [A], [B], and [C] in the following reaction](https://images.collegedunia.com/public/qa/images/content/2025_03_17/Screenshot_058819f71742200255416.jpeg)
![product [A], [B], and [C] in the following reaction](https://images.collegedunia.com/public/qa/images/content/2025_03_17/Screenshot_25adc5291742200411302.jpeg)
![product [A], [B], and [C] in the following reaction](https://images.collegedunia.com/public/qa/images/content/2025_03_17/Screenshot_ca6d85501742200449737.jpeg)
![product [A], [B], and [C] in the following reaction](https://images.collegedunia.com/public/qa/images/content/2025_03_17/Screenshot_5fcadf531742200485208.jpeg)
To identify the products [A], [B], and [C] in the given reaction sequence, let's analyze each step one by one, considering typical organic chemistry transformations involved.
Step 1: Formation of Product [A]
Without the explicit reaction details provided in the image, we'll assume the initial transformation follows a common organic reaction pattern. Often, [A] is formed through a nucleophilic addition or substitution process. Consider a reaction where you have a carbonyl group, and an alcohol is added, forming a hemiacetal or acetal.
Step 2: Formation of Product [B]
The next step could involve further reaction of the intermediate [A] with another reagent to yield [B]. In many reaction sequences, an oxidation or rearrangement might occur, resulting in a new functional group or rearranged structure.
Step 3: Formation of Product [C]
Finally, [B] might undergo a cyclization or additional condensation reaction to form [C]. Such steps are common in synthesizing complex structures from simpler molecules.
Referencing the correct structure as per available choices:
![Correct structure of product [A], [B], and [C] in the reaction sequence](https://images.collegedunia.com/public/qa/images/content/2025_03_17/Screenshot_058819f71742200255416.jpeg)
This structure matches the expected result based on the transformations typical in organic synthesis, considering common functional group interconversions.
Let \( y^2 = 12x \) be the parabola and \( S \) its focus. Let \( PQ \) be a focal chord of the parabola such that \( (SP)(SQ) = \frac{147}{4} \). Let \( C \) be the circle described by taking \( PQ \) as a diameter. If the equation of the circle \( C \) is: \[ 64x^2 + 64y^2 - \alpha x - 64\sqrt{3}y = \beta, \] then \( \beta - \alpha \) is equal to:
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:
Let $ A \in \mathbb{R} $ be a matrix of order 3x3 such that $$ \det(A) = -4 \quad \text{and} \quad A + I = \left[ \begin{array}{ccc} 1 & 1 & 1 \\2 & 0 & 1 \\4 & 1 & 2 \end{array} \right] $$ where $ I $ is the identity matrix of order 3. If $ \det( (A + I) \cdot \text{adj}(A + I)) $ is $ 2^m $, then $ m $ is equal to: