Uses of noble gases with description please. thanks
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Answer:
Explanation:
We are asked to find the mass of a number of platinum (Pt) atoms.
<h3>1. Convert Atoms to Moles </h3>First, we convert atoms to moles using Avogadro's Number or 6.022 × 10²³. This is the number of particles (atoms, molecules, formula units, etc.) in 1 mole of a substance. In this case, the particles are platinum atoms.
We will convert using dimensional analysis so we set up a ratio using the information we know (6.022 × 10²³ platinum atoms in 1 mole of platinum).
We are converting 4.99 ×10²¹ atoms of Pt to moles of Pt, so we multiply by this value.
Flip the ratio so the units of atoms of platinum cancel.
Divide.
Next, we convert moles to grams using the molar mass. This is the mass of 1 mole of a substance. This is found on the Periodic Table because it is equivalent to the atomic mass, but the units are grams per mole instead of atomic mass units. Look up platinum's molar mass.
- Pt: 195.08 g/mol
Set up another ratio using this new information (195.08 grams of Pt in 1 mole of Pt).
Multiply by the number of moles we just calculated.
The units of moles of platinum cancel.
The original measurement of atoms ( 4.99 ×10²¹ ) has 3 significant figures, so our answer must have the same. For the number we found, that is the hundredth place. The 6 in the thousandth place tells us to round the 1 up to a 2.
There are approximately <u>1.62 grams of platinum</u> in 4.99 ×10²¹ atoms of platinum.
The synthesis of Methyl Phenyl Ether is shown below,
The synthesis takes place in two steps,
Step 1: Formation of Sodium Phenoxide:
Phenol being more acidic than Alcohols with pKa ≈ 10 can loose its proton attached to oxygen atom, as the resulting phenoxide ion is stabilized by resonance. Therefore, when phenol is treated with NaOH (bBase) it looses proton and forms Sodium Phenoxide.
Step 2: Formation of Methyl Phenyl Ether:
The Phenoxide ion formed in first step when treated with Dimethyl Sulfate produces Methyl Phenyl Ether through a Williamson's Ether synthesis Reaction. Dimethyl sulfate is a well known alkylating agent when treated with phenols, thiols and amines. Dimethyl sulfate readily transfers the methyl group and forms NaSO₄CH₃.
The reaction is as follow,
The synthesis takes place in two steps,
Step 1: Formation of Sodium Phenoxide:
Phenol being more acidic than Alcohols with pKa ≈ 10 can loose its proton attached to oxygen atom, as the resulting phenoxide ion is stabilized by resonance. Therefore, when phenol is treated with NaOH (bBase) it looses proton and forms Sodium Phenoxide.
Step 2: Formation of Methyl Phenyl Ether:
The Phenoxide ion formed in first step when treated with Dimethyl Sulfate produces Methyl Phenyl Ether through a Williamson's Ether synthesis Reaction. Dimethyl sulfate is a well known alkylating agent when treated with phenols, thiols and amines. Dimethyl sulfate readily transfers the methyl group and forms NaSO₄CH₃.
The reaction is as follow,
Hope this might help a little
