Jose wandered 4 kilometers at 2 kilometers per hour. How long did jose wnader?

Chemistry

1 answer:

Anton [14]3 years ago

7 0

8 kilometer? is that right or explain to me pls.

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Is a computer screen energy transfer or transformation?

yarga [219]

A computer screen is energy transfer

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3 years ago

In Part III, the phenolphthalein indicator is used to monitor the equilibrium shifts of the ammonia/ammonium ion system. The phe

AnnZ [28]

The pink color in the solution fades. Some of the colored indicator ion converts to the colorless indicator molecule.

<h3>Explanation</h3>

What's the initial color of the solution?

$\text{NH}_4\text{Cl}$ is a salt soluble in water. $\text{NH}_4\text{Cl}$ dissociates into ions completely when dissolved.

$\text{NH}_4\text{Cl} \; (aq)\to {\text{NH}_4}^{+} \; (aq) +{\text{Cl}}^{-} \; (aq)$ .

The first test tube used to contain $\text{NH}_4\text{OH}$ . $\text{NH}_4\text{OH}$ is a weak base that dissociates partially in water.

$\text{NH}_4\text{OH} \; (aq) \rightleftharpoons {\text{NH}_4}^{+} \;(aq)+ {\text{OH}}^{-} \; (aq)$ .

There's also an equilibrium between $\text{OH}^{-}$ and ${\text{H}_3\text{O}}^{+}$ ions.

${\text{OH}}^{-}\;(aq) + {\text{H}_3\text{O}}^{+} \;(aq) \to 2\; \text{H}_2\text{O} \;(l)$ .

$\text{OH}^{-}$ ions from $\text{NH}_4\text{OH}$ will shift the equilibrium between $\text{OH}^{-}$ and ${\text{H}_3\text{O}}^{+}$ to the right and reduce the amount of ${\text{H}_3\text{O}}^{+}$ in the solution.

The indicator equilibrium will shift to the right to produce more ${\text{H}_3\text{O}}^{+}$ ions along with the colored indicator ions. The solution will show a pink color.

What's the color of the solution after adding NH₄Cl?

Adding $\text{NH}_4\text{Cl}$ will add to the concentration of ${\text{NH}_4}^{+}$ ions in the solution. Some of the ${\text{NH}_4}^{+}$ ions will combine with $\text{OH}^{-}$ ions to produce $\text{NH}_4\text{OH}$ .

The equilibrium between $\text{OH}^{-}$ and ${\text{H}_3\text{O}}^{+}$ ions will shift to the left to produce more of both ions.

${\text{OH}}^{-}\;(aq) + {\text{H}_3\text{O}}^{+} \;(aq) \to 2\; \text{H}_2\text{O} \;(l)$

The indicator equilibrium will shift to the left as the concentration of ${\text{H}_3\text{O}}^{+}$ increases. There will be less colored ions and more colorless molecules in the test tube. The pink color will fade.

7 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.