Answer: The correct option is ALL OF THE ABOVE.
Explanation:
TITRATION is a type of volumetric analysis which is used for determining the concentration of solutions. In this process a specific volume of a solution is placed in a conical flask by means of a pipette and small quantities of a second solution is slowly added from a burette until the end point is reached. This is determined by a means of an indicator which shows a characteristic colour change.
During titration, the following precautions should be followed to avoid errors and maintain standardisation in the experiment.
--> Any air bubble in the burette and pipette must be removed during measurement
--> the burette tap should be tightened to avoid leakage.
--> Remove the funnel from the burette before taking any reading to avoid errors in reading the volume.
--> use the base solution such as Sodium Hydroxide Solution to rinse the burette after washing with soap and tap water:
• to remove any air bubble and fill it's tip
• to remove any residual liquid from the water and soap solution which may interfere with the results of the experiment.
• to check if the burette is in good condition.
Therefore all of the above options to the question are correct.
I don't know what the options were but a material that is very likely going to be challenging to recognize under a microscope as a mixture is a homogeneous mixture. A homogenous mixture is uniform and thus hard to recognize as a mixture. An example is water!
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Answer:
2-ethoxy-2-methylpropan-1-ol
Explanation:
On this reaction, we have an "<u>epoxide"</u> (2-methyl-1,2-epoxypropane). Additionally, we have <u>acid medium</u> (due to the sulfuric acid
). The acid medium will produce the <u>hydronium ion</u> (
). This ion would be attacked by the oxygen of the epoxide. Then a <u>carbocation</u> would be produced, in this case, the most stable carbocation is the <u>tertiary one</u>. Then an <u>ethanol</u> molecule acts as a nucleophile and will attack the carbocation. Finally, a <u>deprotonation </u>step takes place to produce <u>2-ethoxy-2-methylpropan-1-ol</u>.
See figure 1
I hope it helps!