Answer:
Kc = 50.5
Explanation:
We determine the reaction:
H₂ + I₂ ⇄ 2HI
Initially we have 0.001 molesof H₂
and 0.002 moles of I₂
If we have produced 0.00187 moles of HI in the equilibrium we have to know, how many moles of I₂ and H₂, have reacted.
H₂ + I₂ ⇄ 2HI
In: 0.001 0.002 -
R: x x 2x
Eq: 0.001-x 0.002-x 0.00187
x = 0.00187/2 = 9.35×10⁻⁴ moles that have reacted
So in the equilibrium we have:
0.001 - 9.35×10⁻⁴ = 6.5×10⁻⁵ moles of H₂
0.002 - 9.35×10⁻⁴ = 1.065×10⁻³ moles of I₂
Expression for Kc is = (HI)² / (H₂) . (I₂)
0.00187 ² / 6.5×10⁻⁵ . 1.065×10⁻³ = 50.5
Element on the right side of the periodic table differ from the elements on the left side in that elements on the <em>right side are non metallic and tends to be gases at room temperature.</em>
<em> </em><u>Explanation</u>
In the periodic table there element in the right side , left side and those which are in between.
- Example of element in the right side is fluorine chlorine, neon, Argon among others.
- This element have higher effective nuclear charges and stabilize electrons more effectively.
- there electrostatic intermolecular forces are generally weak therefore they exist in liquid or gaseous state.
Answer:
The rapid movement of excess charge from one place to another is an <em>electric discharge.</em>
Explanation:
A material in which electrons <em>CANNOT</em> move easily from place to place is an insulator. A material in which electrons <em>CAN </em>move easily from place to place is a conductor.
h2+o2=2h2o.................................................
2-bromo-1-chloro-4-nitrobenzene is being synthesized in following sequence:
Step 1: Chlorination of Benzene:
This is Halogenation reaction of benzene. In this step benzene is reacted with Chlorine gas in the presence of lewis acid (i.e. FeCl₃). This results in the formation of Chlorobenzene as shown in red step below.
Step 2: Nitration of Chlorobenzene:
The chlorine atom on benzene has a ortho para directing effect. Therefore, the nitration of chlorobenzene will yield para nitro chlorobenzene as shown in blue step below.
Step 3: Bromination of 1-chloro-4-nitrobenzene:
In this step bromination is done by reacting bromine in the presence of lewis acid. The chlorine being ortho para directing in nature and nitro group being meta directing in nature will direct the incoming Br⁺ (electrophile) to the desired location. Hence, 2-bromo-1-chloro-4-nitrobenzene is synthesized in good yield.
