Answer:
1) When 6.97 grams of sodium(s) react with excess water(l), 56.0 kJ of energy are evolved.
2) When 10.4 grams of carbon monoxide(g) react with excess water(l), 1.04 kJ of energy are absorbed.
Explanation:
1) The following thermochemical equation is for the reaction of sodium(s) with water(l) to form sodium hydroxide(aq) and hydrogen(g).
2 Na(s) + 2H₂O(l) ⇒ 2NaOH(aq) + H₂(g) ΔH = -369 kJ
The enthalpy of the reaction is negative, which means that 369 kJ of energy are evolved per 2 moles of sodium. The energy evolved for 6.97 g of Na (molar mass 22.98 g/mol) is:
2) The following thermochemical equation is for the reaction of carbon monoxide(g) with water(l) to form carbon dioxide(g) and hydrogen(g).
CO(g) + H₂O(l) ⇒ CO₂(g) + H₂(g) ΔH = 2.80 kJ
The enthalpy of the reaction is positive, which means that 2.80 kJ of energy are absorbed per mole of carbon monoxide. The energy evolved for 10.4 g of CO (molar mass 28.01 g/mol) is:
Explanation:
the conductors are the three u have checked
Answer:
The absorbance of the myoglobin solution across a 1 cm path is 0.84.
Explanation:
Beer-Lambert's law :
Formula used :
where,
A = absorbance of solution
c = concentration of solution
= Molar absorption coefficient
l = path length
= incident light
= transmitted light
Given :
l = 1 cm, c = 1 mg/mL ,
Molar mass of myoglobin = 17.8 kDa = 17.8 kg/mol=17800 g/mol
(1 Da = 1 g/mol)
c = 1 mg /mL = 
1 mg = 0.001 g, 1 mL = 0.001 L
The absorbance of the myoglobin solution across a 1 cm path is 0.84.
As the building blocks of proteins , amino acids are linked to almost every life process, but they also have key roles as precursor compounds in many physiological processes.
Answer:
Explanation has been given below
Explanation:
- In diaxial conformation of cis-1,3-disubstituted cyclohexane, 4 gauche-butane interactions along with syn-diaxial interaction are present. Hence it readily gets converted to diequitorial conformation where no such gauche-butane interaction is present
- In two possible conformations of trans-1,3-disubstituted cyclohexane, 2 gauche-butane interactions are present in each of them.
- Hence cis-1,3-disubstituted cyclohexane exists almost exclusively in diequitorial form. But trans-1,3-disubstituted cyclohexane has no such option.
- Trans-1,3-disubstituted cyclohexane experiences gauche butane interaction in each of the two conformations.
- Therefore cis-1,3-disubstituted cyclohexane is more stable than trans conformation
