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liberstina [14]
3 years ago
5

Rabbits are best described as _______.

Chemistry
1 answer:
Otrada [13]3 years ago
7 0

Answer:  its actually primary consumers

Explanation:

You might be interested in
HC2H3O2 (aq) + H2O (l) ⇔ C2H3O2- (aq) + H3O+ (aq) Ka = 1.8 x 10-5
marin [14]

The concentration of [H3O⁺]=2.86 x 10⁻⁶ M

<h3>Further explanation</h3>

In general, the weak acid ionization reaction  

HA (aq) ---> H⁺ (aq) + A⁻ (aq)  

Ka's value  

\large {\boxed {\bold {Ka \: = \: \frac {[H ^ +] [A ^ -]} {[HA]}}}}

Reaction

HC₂H₃O₂ (aq) + H₂O (l) ⇔  (aq) + H₃O⁺ (aq) Ka = 1.8 x 10⁻⁵

\tt Ka=\dfrac{[C_2H_3O^{2-}[H_3O^+]]}{[HC_2H_3O_2]}}\\\\1.8\times 10^{-5}=\dfrac{0.22\times [H_3O^+]}{0.035}

[H₃O⁺]=2.86 x 10⁻⁶ M

5 0
3 years ago
Match the vocabulary with the definitions.
Fiesta28 [93]

1: Decomposition reaction
2: Combination reaction
3: product
4: Reactant
8 0
2 years ago
If an object is accelerating the forces acting on the object are ?​
belka [17]

Answer:

If an object is accelerating the forces acting on the object are BALANCED.

Explanation

if an object is moving at a constant rate of acceleration, the the forces acting upon it are balanced .

7 0
3 years ago
What are some bad thing jellyfish do?
True [87]
Jellyfish aren't necessarily bad or do bad things humans do find that the tentacles that happen to "shock" or "electructe" people are bad. As well as the way jellyfish live in one grouping it is rare but you can find jellyfish out of a group, they do this that way they can eat and stay away from predators.


I hope this helped you!
3 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
3 years ago
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