Answer:
Final concentration of NaOH = 0.75 M
Explanation:
For 
:-
Given mass = 90.0 g
Molar mass of NaOH = 39.997 g/mol
The formula for the calculation of moles is shown below:
Thus,
Molarity is defined as the number of moles present in one liter of the solution. It is basically the ratio of the moles of the solute to the liters of the solution.
The expression for the molarity, according to its definition is shown below as:
Where, Volume must be in Liter.
It is denoted by M.
Given, Volume = 3.00 L
So,
<u>Final concentration of NaOH = 0.75 M</u>
Answer:
Ionic compound are when electrons are given to another element, making one atom positive and the other negative, so they attract. Covalent compound is when both atoms share electrons with each other.
Answer: A. an electron
<u>Beta particles are electrons or positrons (electrons with positive electric charge or antielectrons).</u> Beta decay is a type of radioactive decay in which a beta ray is emitted from an atomic nucleus.
<u>Beta decay occurs when, in an unstable nucleus with too many protons or too many neutrons, one of the protons or neutrons transforms into the other.</u> In beta minus decay, a neutron is broken down into a proton, an electron, and an antineutrino (the neutrino antiparticle, meaning it has an opposite charge to the neutrino). In beta decay plus, a prototype breaks down into a neutron, a positron and a neutrino.
True. Mitosis is a part of the call cycle when replicated chromosomes are separated into new nuclei. It is a for if eukaryotic cell division that produces two daughter cells with the same genetic components as the parent cells.
Answer:
A noncompetitive inhibitor can only bind to an enzyme with or without a substrate at several places at a particular point in time
Explanation:
this is because It changes the conformation of an enzyme as well as its active site, which makes the substrate unable to bind to the enzyme effectively so that the efficiency of the enzyme decreases. A noncompetitive inhibitor binds to the enzyme away from the active site, altering/distorting the shape of the enzyme so that even if the substrate can bind, the active site functions less effectively and most of the time also the inhibitor is reversible
