Answer:
<h2>1. Ionic compound-
</h2><h2>2. Polar molecular compound-
</h2>
Explanation:
Mg is a metal that has 12 atomic numbers and thus its electronic configuration is 
. The outer most shell of this element has 2 electrons so it loses 2 electrons and thus form 
ions. Br is a nonmetal and has 35 atomic number so its electronic configuration is 
. Since its outermost shell has 7 electrons so it can accept one electron and thus forms 
. So magnesium ion and bromide ion combine and forms an ionic compound .
P is also a nonmetal and combine with Br with covalent bond and due to electronegativity differences form polar covalent compound such as .
On temperature 25°C (298,15K) and pressure of 1 atm each gas has same amount of substance:
n(gas) = p·V ÷ R·T = 1 atm · 20L ÷ <span>0,082 L</span>·<span>atm/K</span>·<span>mol </span>· 298,15 K
n(gas) = 0,82 mol.
1) m(He) = 0,82 mol · 4 g/mol = 3,28 g.
d(He) = 10 g + 3,28 g ÷ 20 L = 0,664 g/L.
2) m(Ne) = 0,82 mol · 20,17 g/mol = 16,53 g.
d(Ne) = 26,53 g ÷ 20 L = 1,27 g/L.
3) m(CO) = 0,82 mol ·28 g/mol = 22,96 g.
d(CO) = 32,96 g ÷ 20L = 1,648 g/L.
4) m(NO) = 0,82 mol ·30 g/mol = 24,6 g.
d(NO) = 34,6 g ÷ 20 L = 1,73 g/L.
The rate of Formation of Carbocation mainly depends on two factors'
1) Stability of Carbocation: The ease of formation of Carbocation mainly depends upon the ionization of substrate. If the forming carbocation id tertiary then it is more stable and hence readily formed as compared to secondary and primary.
2) Ease of detaching of Leaving Group: The more readily and easily the leaving group leaves the more readily the carbocation is formed and vice versa. In given scenario the carbocation formed is tertiary in all three cases, the difference comes in the leaving group. So, among these three substrates the one containing Iodo group will easily dissociate to form tertiary carbocation because due to its large size Iodine easily leaves the substrate, secondly Chlorine is a good leaving group compared to Fluoride. Hence the order of rate of formation of carbocation is,
R-I > R-Cl > R-F
B > C > A
Assume that the amount needed from the 5% acid is x and that the amount needed from the 6.5% acid is y.
We are given that:
The volume of the final solution is 200 ml
This means that:
x + y = 200
This can be rewritten as:
x = 200 - y .......> equation I
We are also given that:
The concentration of the final solution is 6%
This means that:
5%x + 6.5%y = 6% (x+y)
This can be rewritten as:
0.05 x + 0.065 y = 0.06 (x+y) ............> equation II
Substitute with equation I in equation II and solve for y as follows:
0.05 x + 0.065 y = 0.06 (x+y)
0.05 (200-y) + 0.065 y = 0.06 (200-y+y)
10 - 0.05 y + 0.065 y = 12
0.015y = 12-10 = 2
y = 2/0.015
y = 133.3334 ml
Substitute with the y in equation I to get the x as follows:
x = 200 - y
x = 200 - 133.3334
x = 66.6667 ml
Based on the above calculations:
The amount required from the 5% acid = x = 66.6667 ml
The amount required from the 6.5% acid = y = 133.3334 ml
Hope this helps :)
Answer:
See explanation
Explanation:
% optical purity = specific rotation of mixture/specific rotation of pure enantiomer * 100/1
specific rotation of mixture = 23°
specific rotation of pure enantiomer = 61°
Hence;
% optical purity = 23/61 * 100 = 38 %
More abundant enantiomer = 100% - 38 % = 62%
Hence the pure (S) carvone is (-) 62° is the more abundant enantiomer.
Enantiomeric excess = 62 - 50/50 * 100 = 24%
Hence
(R) - carvone = 38 %
(S) - carvone = 62%
