Basic radicals (cations) have been divided into groups based on Ksp values
Answer:
they are equal
Explanation:
the Law of Conservation of Mass states that for any system closed to all transfers of matter and energy, the mass of the system must remain constant over time, as the system's mass cannot change
We use the osmotic pressure to determine the concentration of the solute in the solution. Then, we multiply the volume of the solution to determine the number of moles of solute particles. We need to establish to equations since we have two unknowns, the mass of of each solute. We do as follows:
osmotic pressure = CRT
<span>C = 7.75 / 0.08205 (296.15) = 0.3189 mol / L</span>
<span>moles of particles = C*V = 0.3189*0.250 =0.0797 mol </span>
<span>0.0797 = moles of sucrose + 2*moles of salt </span>
<span>x + 2y = 0.0797 </span>
<span>and </span>
<span>x(MMsucrose) + y(MMNaCl) = 10.2</span>
<span>342x + 58.5y = 10.2
</span>
<span>solve for x and y
</span>
<span>x = 0.0252 mol sucrose</span>
<span>y = 0.0273 mol NaCl
</span>
<span>mass Sucrose = 0.0252(342) = 8.6184 g </span>
<span>mass NaCl = 0.0273(58.5) = 1.5971 g </span>
<span>% NaCl = (1.5971 / 10.2)*100 = 15.66%</span>
Because the Potassium ion loses an electron, the electrons come a little closer to the nucleus because they are attracted to the protons. This makes the ion smaller in radius
Answer:but-1-ene
Explanation:This is an E2 elimination reaction .
Kindly refer the attachment for complete reaction and products.
Sodium tert-butoxide is a bulky base and hence cannot approach the substrate 2-chlorobutane from the more substituted end and hence major product formed here would not be following zaitsev rule of elimination reaction.
Sodium tert-butoxide would approach from the less hindered side that is through the primary centre and hence would lead to the formation of 1-butene .The major product formed in this reaction would be 1-butene .
As the mechanism of the reaction is E-2 so it will be a concerted mechanism and as sodium tert-butoxide will start abstracting the primary hydrogen through the less hindered side simultaneously chlorine will start leaving. As the steric repulsion in this case is less hence the transition state is relatively stabilised and leads to the formation of a kinetic product 1-butene.
Kinetic product are formed when reactions are dependent upon rate and not on thermodynamical stability.
2-butene is more thermodynamically6 stable as compared to 1-butene
The major product formed does not follow the zaitsev rule of forming a more substituted alkene as sodium tert-butoxide cannot approach to abstract the secondary proton due to steric hindrance.