Answer:
222.30 L
Explanation:
We'll begin by calculating the number of mole in 100 g of ammonia (NH₃). This can be obtained as follow:
Mass of NH₃ = 100 g
Molar mass of NH₃ = 14 + (3×1)
= 14 + 3
= 17 g/mol
Mole of NH₃ =?
Mole = mass /molar mass
Mole of NH₃ = 100 / 17
Mole of NH₃ = 5.88 moles
Next, we shall determine the number of mole of Hydrogen needed to produce 5.88 moles of NH₃. This can be obtained as follow:
N₂ + 3H₂ —> 2NH₃
From the balanced equation above,
3 moles of H₂ reacted to produce 2 moles NH₃.
Therefore, Xmol of H₂ is required to p 5.88 moles of NH₃ i.e
Xmol of H₂ = (3 × 5.88)/2
Xmol of H₂ = 8.82 moles
Finally, we shall determine the volume (in litre) of Hydrogen needed to produce 100 g (i.e 5.88 moles) of NH₃. This can be obtained as follow:
Pressure (P) = 95 KPa
Temperature (T) = 15 °C = 15 + 273 = 288 K
Number of mole of H₂ (n) = 8.82 moles
Gas constant (R) = 8.314 KPa.L/Kmol
Volume (V) =?
PV = nRT
95 × V = 8.82 × 8.314 × 288
95 × V = 21118.89024
Divide both side by 95
V = 21118.89024 / 95
V = 222.30 L
Thus the volume of Hydrogen needed for the reaction is 222.30 L
Answer: Induced Fit
Explanation: The process wherein the enzymes change their shape is called as induced fit. It is the precision aligning of enzymes essential for catalytic activity which is caused by the binding of the substrate as enzymes possess active sites. Hence, as the substrate approaches the enzymes, the enzyme alters its shape.
Answer:
Sucrose is a disaccharide composed of alpha D gluose and beta D fructose linked together by beta 2,alpha1 glycosidic linkage.
Explanation:
The specificity of glycosidic linkage very much essential to choose the substrate for the synthesis of specific disaccharide.
For example sucrose contain beta 2,alpha1 glycosidic linkage that means the hydroxyl group of anomeric carbon of one monosaccharide(fructose) should remain in beta conformation and the hydroxyl group of other monosaccharide(glucose) should remain in alpha conformation.
Markovnikov rule, in organic chemistry, a generalization, formulated by Vladimir Vasilyevich Markovnikov in 1869, stating that in addition reactions to unsymmetrical alkenes, the electron-rich component of the reagent adds to the carbon atom with fewer hydrogen atoms bonded to it, while the electron-deficient component ...