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Vesna [10]
4 years ago
12

Need suggestions on where water is naturally found. I have to make an A-Z list and I already have a few but was wondering if any

one could come up with new ideas.
Chemistry
1 answer:
Mrrafil [7]4 years ago
3 0
Arcapellago
bay
cave
ditch (water collection from rain)
estuary
Gyser
lake
marsh
pond

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A solution of H2SO4(aq) with a molal concentration of 4.80 m has a density of 1.249 g/mL. What is the molar concentration of thi
Naddika [18.5K]
Imagine we have <span>mass of solvent 1kg (1000g)
According to that: </span>molality =n(solute) / m(solvent) =\ \textgreater \  4.8m = 4.8mole / 1kg
= 4.8 mole * 98 g/mole = 470g
m(H2SO4) = n(H2SO4)*Mr(H2SO4) =\ \textgreater \=\ \textgreater \  Molarity = 4.8 mole / 1.2 L = 4 M m(H2SO4)  which is =<span>470g

</span><span>m(solution) = m(H2SO4) + m(solvent) = 470 + 1000 = 1470 g
d(solution) = m(solution) / V(solution) =>
=> 1.249 g/mL = 1470 g / V(solution) =></span>
Molarity = n(solute) / V(solution) =\ \textgreater \
5 0
3 years ago
In the absence of sodium methoxide, the same alkyl bromide gives a different product. Draw an arrowpushing mechanism to account
hoa [83]

Answer:

See explanation below

Explanation:

The question is incomplete, cause you are not providing the structure. However, I found the question and it's attached in picture 1.

Now, according to this reaction and the product given, we can see that we have sustitution reaction. In the absence of sodium methoxide, the reaction it's no longer in basic medium, so the sustitution reaction that it's promoted here it's not an Sn2 reaction as part a), but instead a Sn1 reaction, and in this we can have the presence of carbocation. What happen here then?, well, the bromine leaves the molecule leaving a secondary carbocation there, but the neighbour carbon (The one in the cycle) has a more stable carbocation, so one atom of hydrogen from that carbon migrates to the carbon with the carbocation to stabilize that carbon, and the result is a tertiary carbocation. When this happens, the methanol can easily go there and form the product.

For question 6a, as it was stated before, the mechanism in that reaction is a Sn2, however, we can have conditions for an E2 reaction and form an alkene. This can be done, cause the extoxide can substract the atoms of hydrogens from either the carbon of the cycle or the terminal methyl of the molecule and will form two different products of elimination. The product formed in greater quantities will be the one where the negative charge is more stable, in this case, in the primary carbon of the methyl it's more stable there, so product 1 will be formed more (See picture 2)

For question 6b, same principle of 6a, when the hydrogen migrates to the 2nd carbocation to form a tertiary carbocation the methanol will promove an E1 reaction with the vecinal carbons and form two eliminations products. See picture 2 for mechanism of reaction.

3 0
4 years ago
When wood burns, the mass of the ash is less than the mass of the original wood. Yet the law of conservation of matter says that
satela [25.4K]

Explanation:

According to the law of the conservation of mass, 'mass is conserved in a chemical reaction. The mass cannot be created nor be destroyed in a chemical process'.

This law holds true for the burning of wood also. Although the wood burns to produce ash which weighs less than wood but also, it produces some soot and other gases and the sum of the masses of all these is equal to the sum of the masses of wood and oxygen that reacted with it.

7 0
3 years ago
A reaction between an acid and a base produced lithium chloride (LiCl). What acid and base combination could produce this salt?
dolphi86 [110]

C sulfuric acid and  magnesium hydroxide

5 0
3 years ago
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A combustion reaction is one type of what class of reactions?
ivanzaharov [21]
It is a. oxidation-reduction
6 0
3 years ago
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