





are not benzenoid compounds, since benzenoid compound contains benzene ring.
1 gram of sodium hydroxide was treated with 25 ml. of 0.75 M HCI solution, the mass of sodium hydroxide left unreacted is equal to :
Identify Z in the following reaction sequence.

 
| List-I  | List-II  | ||
| (A) | NH3 | (I) | Trigonal Pyramidal | 
| (B) | BrF5 | (II) | Square Planar | 
| (C) | XeF4 | (III) | Octahedral | 
| (D) | SF6 | (IV) | Square Pyramidal | 
Uniform magnetic fields of different strengths $ B_1 $ and $ B_2 $, both normal to the plane of the paper, exist as shown in the figure. A charged particle of mass $ m $ and charge $ q $, at the interface at an instant, moves into region 2 with velocity $ v $ and returns to the interface. It continues to move into region 1 and finally reaches the interface. What is the displacement of the particle during this movement along the interface?
Consider the velocity of the particle to be normal to the magnetic field and  $ B_2 > B_1 $.
For a given reaction \( R \rightarrow P \), \( t_{1/2} \) is related to \([A_0]\) as given in the table. Given: \( \log 2 = 0.30 \). Which of the following is true? 
 
| \([A]\) (mol/L) | \(t_{1/2}\) (min) | 
|---|---|
| 0.100 | 200 | 
| 0.025 | 100 | 
A. The order of the reaction is \( \frac{1}{2} \). 
B. If \( [A_0] \) is 1 M, then \( t_{1/2} \) is \( 200/\sqrt{10} \) min. 
C. The order of the reaction changes to 1 if the concentration of reactant changes from 0.100 M to 0.500 M. 
D. \( t_{1/2} \) is 800 min for \( [A_0] = 1.6 \) M. 
The three structural formulas – complete structure, condensed structure, and bond line structural formulas are explained below:
The Lewis dot structure is considered as the complete structural formula. In Lewis structure, the covalent bonds in the compound are denoted by a dash (―). This helps to emphasize the number of bonds formed by the electrons. Every single bond, a double bond, and a triple bond are represented by one dash, double dash, and triple dash respectively. It illustrates every single bond formed between every atom in the compound, thus called complete structural formula.
Since complete structural formula consumes much time and space to represent the structure, we can condense them. This is the condensed structural formula, where replacing some dashes/bonds by a number of identical groups attached to an atom by a subscript.
A bond lines structural formula is another way of structural representation of organic compounds. Here, every bond is represented as a line in a zigzag manner. If not specified, every terminal is assumed to be a methyl (-CH3) group.