The level in the beaker will increase because the volumes of the spheres will also be added to the volume of the water. First, we must determine the volume of each sphere. For this, we will use:
density = mass / volume
We can check the density of both aluminum and iron in literature, and given the mass, we may obtain the volume.
Aluminum:
Density = 2.70 g/ml
Mass = 20.4 g
Volume = 20.4 / 2.7 = 7.56 ml
Iron:
Density = 7.87 g/ml
Mass = 49.4 g
Volume = 49.4 / 7.87 = 6.28 ml
Now, we add these volumes to the volume of water present:
75.2 + 6.28 + 7.56 = 89.04
The new level will be 89.0 ml
Zinc would be considered the strongest reducing agent.
<h3>Reducing agent</h3>
A reducing agent is a chemical species that "donates" one electron to another chemical species in chemistry (called the oxidizing agent, oxidant, oxidizer, or electron acceptor). Earth metals, formic acid, oxalic acid, and sulfite compounds are a few examples of common reducing agents.
Reducers have excess electrons (i.e., they are already reduced) in their pre-reaction states, whereas oxidizers do not. Usually, a reducing agent is in one of the lowest oxidation states it can be in. The oxidation state of the oxidizer drops while the oxidizer's oxidation state, which measures the amount of electron loss, increases. The agent in a redox process whose oxidation state rises, which "loses/donates electrons," which "oxidizes," and which "reduces" is known as the reducer or reducing agent.
Learn more about reducing agent here:
brainly.com/question/2890416
#SPJ4
<h3 />
Answer:
(BH3 follows the octet rule by dimerizing, as Hadi Kurniawan AR pointed out.) For H and He, an "octet" = 2 electrons. Boron does prefer to follow the octet rule, in that it likes to form borate compounds such as NaBH4. It also is happy to form compounds with elements with lone pairs.
Anions are solvated in protic hydrogen-bonding solvents (such as ethanol). Consequently, nucleophiles are less reactive. Since soft nucleophiles are less strongly solvated than hard nucleophiles, these solvents boost the relative reactivity of soft anions.
<h3>
Ethanol is either a nucleophile or a base.</h3>
The ethanol is a base Because carbocation is an extremely reactive species, a base or nucleophile as weak as ethanol can replace or remove it. SN1 and E1 would not be conceivable without the carbocation or a strong departing group.
<h3>How do solvents impact anionic nucleophile's reactivity?</h3>
In polar aprotic solvents, nucleophilic substitution reactions of anionic nucleophiles often proceed more quickly. The normal relative reactivity order in such solvents (like DMSO)is Anions are solvated in protic hydrogen-bonding solvents (such as ethanol). Consequently, nucleophiles are less reactive.
Learn more about nucleophiles here:-
brainly.com/question/27127109
#SPJ4
