Answer:
68,2%
Explanation:
Supposing the initial salt concentration of lake Parsons is the same of non-isolated lakes, 6,67L, and the change of salt concentration in isolated lake is just for water evaporation it is possible to write:
6,67gL⁻¹×X = 21gL⁻¹×Y
<em>-Where X is the initial water and Y is the water that remains in the isolated lake-</em>
Thus:
6,67X = 21Y
0,318 = Y/X
0,318 is the ratio of water that remains between total water. To obtain the ratio of evaporated water:
1-0,318 = 0,682
In percentage: <em>68,2%</em>
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I hope it helps!
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The alkali metals can't exist alone in nature because of incomplete outermost shell of alkali metals.
<h3>What are the properties of alkali metals?</h3>
The alkali metals have the high thermal and electrical conductivity. It has high lustre, ductility, and malleability as compared to other materials. Each alkali metal atom has one electron in its outermost shell which make more reactive.
So we can conclude that the alkali metals can't exist alone in nature because of incomplete outermost shell of alkali metals.
Learn more about metal here: brainly.com/question/25597694
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Answer:
The answer to your question is 1 M
Explanation:
Data
Molarity = ?
mass of CaCl₂ = 222.2 g
Volume = 2 l
Process
1.- Calculate the molar mass of CaCl₂
CaCl₂ = 40 + (35.5 x 2) = 40 + 71 = 111 g
2.- Calculate the moles of CaCl₂
111g of CaCl₂ ---------------- 1 mol
222.2 f of CaCl₂ ---------------- x
x = (222.2 x 1) / 111
x = 222.2 / 111
x = 2 moles
3.- Calculate the Molarity
Molarity = moles / Volume
-Substitution
Molarity = 2/2
-Result
Molarity = 1
Answer:
1) acetylide
2) enol
3) aldehydes
4) tautomers
5) alkynes
6) Hydroboration
7) Keto
8) methyl ketones
Explanation:
Acetylide anions (R-C≡C^-) is a strong nucleophile. Being a strong nucleophile, we can use it to open up an epoxide ring by SN2 mechanism. The attack of the acetylide ion occurs from the backside of the epoxide ring. It must attack at the less substituted side of the epoxide.
Oxomercuration of alkynes and hydroboration of alkynes are similar reactions in that they both yield carbonyl compounds that often exhibit keto-enol tautomerism.
The equilibrium position may lie towards the Keto form of the compound. Usually, if terminal alkynes are used, the product of the reaction is a methyl ketone.
