Answer:
e
Explanation:
<em>Provided the reaction that leads to the formation of the products can proceed in both forward and backward directions, the correct answer would be yes because the reaction will proceed backward until equilibrium is reached.</em>
<u>For a reaction that can proceed both forward and backward, the addition of a catalyst increases the rate of reaction in both directions based on the fact that a catalyst cannot alter the equilibrium of a reaction. </u>
Hence, if an enzyme is added to the product of a reaction that has the potential to proceed in both forward and reverse reactions, a substrate would be expected to form because the reaction will proceed backward until an equilibrium is reached.
The correct option is e.
Answer:
2-chloro-4-methylpentanal.
Explanation:
Hello there!
In this case, according to the chemical compound:
CH3-CH-CH2-CH-CHO
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CH3 Cl
We can see the main functional group is an starting carbonyl, which means this is an aldehyde. Moreover, we can see a Cl-substituent on the second carbon and a methyl substituent on the fourth carbon. Therefore, the IUPAC name turns out: 2-chloro-4-methylpentanal.
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Petrol is a conductor of electricity, because it conducts rather than insulates.
Answer:
B
Explanation:
Look on the x-axis for the tick marked "60". This indicates 60 degrees Celsius, which we want. Now, look on the y-axis for the tick marked "60". This indicates 60 grams of 
. Trace along the graph to find where these two places meet at (60, 60).
Now, look for the solubility curve of ; it's the yellow-orange line. Find out what the y-coordinate of the point where x = 60 is on the line: it's around (60, 65).
So, since the point (60, 60) is below the line corresponding to this substance, is unsaturated.
The answer is B.
