Answer:
2 H2(g) + O2(g) → 2 H2O(ℓ) ΔH = −570 kJ
Explanation:
Answer:
Its high polarity
Explanation:
Solvent is the that part of solution which is present in large proportion and have ability to dissolve the solute. In simplest form it is something in which other substance get dissolve. The most widely used solvent is water, other examples are toluene, acetone, ethanol, chloroform etc.
Water is called universal solvent because of high polarity all polar substance are dissolve in it. Hydrogen is less electronegative while oxygen is more electronegative and because of difference in electronegativity hydrogen carry the partial positive charge while oxygen carry partial negative charge.
Water create electrostatic interaction with other polar molecules. The negative end of water attract the positive end of polar molecules and positive end of water attract negative end of polar substance and in this way polar substance get dissolve in it.
Example:
when we stir the sodium chloride into water the cation Na⁺ ions are surrounded by the negative end of water i.e oxygen and anion Cl⁻ is surrounded by the positive end of water i.e hydrogen and in this way all salt is get dissolved.
Explanation:
Molarity is defined as number of moles per liter of solution.
Mathematically, molarity = 
It is given that molarity is 0.0800 M and volume is 50.00 mL or 0.05 L.
molarity = 
0.0800 M = 
no. of moles = 1.6 mol
Therefore, molar mass of cupric sulfate pentahydrate is 249.68 g/mol. So, calculate the mass as follows.
No. of moles = 
mass in grams = 
= 
= 399.488 g
Thus, we can conclude that 399.488 g of cupric sulfate pentahydrate are needed to prepare 50.00 mL of 0.0800M CuSO4× 5H2O.
Thin layer chromatography(TLC) works with the principle of separation through adsorption.
It is used in the isolation and extraction of lipids through the following steps:
- apply the lipid samples spots in the bottom of the plate.
- also apply sample solution to the marked spot
- pour the mobile phase into the TLC chamber and use a moist filter paper to cover it. this is done to maintain equal humidity.
- then place the plate in the TLC chamber and close it with a lid.
- the plate is immersed into the solvent (mobile phase) for its development. this is done, keeping in mind that the sample spot should be above the solvent.
- once the sample spots are developed, they are removed and dried.
- this is later viewed using the UV light chamber to see the isolation of the lipid sample.
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