<span>In the field of science, usually, the product of an experiment is
computed ahead to understand if it reached a specific objective. It would reach
greater than 100% of percent yield if the factors include faster reaction rates;
proper handling of the reactants, no outside contaminants, and the procedure of
the experiment is followed smoothly. It would reach lesser than 100% percent yield
if the experiment is not followed, external factors such as contamination from
the environment (wind, moisture, etc). </span>
The answer should be hydrogen bonding. Water only has oxygen and hydrogen in it, which are both nonmetals, so you know the answer cannot be metallic or ionic. It also cannot be nonpolar because the electronegativity of the oxygens will make the molecule polar. You can also know it is hydrogen bonding because it can only take place when a hydrogen is attached to an oxygen, fluorine, or nitrogen. These bonds are very strong attractions, so the molecules are extremely hard to pull apart, creating a high boiling point. Hope that helps!
Blood.
<span>Blood is heterogeneous because it has corpuscles (blood cells and platelets) physically suspended in blood plasma. Blood plasma and the corpuscles have different properties and can be separated by methods such as centrifugation. Also, blood is considered a colloid suspension because it has the properties of both a colloid and a suspension. This is because the blood plasma acts as a colloid. More so, if blood was left to settle,then the blood cells would collect at the bottom hence taking the characteristic of a suspension. </span>
<span>Salad dressing.</span>
<span>Depending on the type of salad, it can either be a heterogeneous or homogeneous mixture. If the salad dressing is only of vinegar or any other oil, then it is a homogenous mixture. However, if it involves a mixture of vinegar and other oils, pepper, herbs, and etcetera, then it is a heterogeneous mixture</span>
Answer:
Nitrobenzene is too deactivated (by the nitro group) to undergo a Friedel-Crafts alkylation.
Explanation:
The benzene ring in itself does not easily undergo electrophilic substitution reaction. Some groups activate or deactivate the benzene ring towards electrophilic substitution reactions.
-NO2 ia a highly deactivating substituent therefore, Friedel-Crafts alkylation of nitrobenzene does not take place under any conditions.
This reaction scheme is therefore flawed because Nitrobenzene is too deactivated (by the nitro group) to undergo a Friedel-Crafts alkylation.
