PH is defined as the negative log of Hydrogen ion concentration. Mathematically we can write this as:
![pH=-log[H^{+}]=-log[H_{3}O]](https://tex.z-dn.net/?f=pH%3D-log%5BH%5E%7B%2B%7D%5D%3D-log%5BH_%7B3%7DO%5D%20%20)
We are given the concentration of
. Using the value in formula, we get:
![pH=-log[1.8*10^{-4}]=3.745](https://tex.z-dn.net/?f=pH%3D-log%5B1.8%2A10%5E%7B-4%7D%5D%3D3.745%20)
Therefore, the pH of the solution will be 3.745
If one or more nucleotide pairs are deleted from a DNA strand, this is known as a frameshift mutation
<h3>
Define Frameshift Mutation</h3>
Insertions or deletions in the genome that are not multiples of three nucleotides are referred to as frameshift mutations. They are a particular class of insertion-deletion (indel) alterations that are present in polypeptides' coding sequences. Here, there are no multiples of three in the number of nucleotides that are added to or subtracted from the coding sequence. They may result from really basic alterations like the insertion or deletion of a single nucleotide.
<h3>
Frameshift mutations' effects</h3>
One of the most harmful modifications to a protein's coding sequence is a frameshift mutation. They are quite prone to produce non-functional proteins that frequently interfere with a cell's metabolic processes and result in significant alterations to polypeptide length and chemical makeup. Frameshift mutations can cause the mRNA to stop translating too soon and create an extended polypeptide.
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The correct option is (b)
NaNH2 is an effective base. It can be a good nucleophile in the few situations where its strong basicity does not have negative side effects. It is employed in elimination reactions as well as the deprotonation of weak acids.Alkynes, alcohols, and a variety of other functional groups with acidic protons, such as esters and ketones, will all be deprotonated by NaNH2, a powerful base.Alkynes are deprotonated with NaNH2 to produce what are known as "acetylide" ions. These ions are powerful nucleophiles that can react with alkyl halides to create carbon-carbon bonds and add to carbonyls in an addition reaction.Acid/base and nucleophilic substitution are the two types of reactions.Using the right base, terminal alkynes can be deprotonated to produce a carbanion.A good C is the acetylide carbanion.The acetylide carbanion can undergo nucleophilic substitution reactions because it is a potent C nucleophile. (often SN2) with 1 or 2 alkyl halides with electrophilic C to create an internal alkyne (Cl, Br, or I).Elimination is more likely to occur with 3-alkyl halides.It is possible to swap either one or both of the terminal H atoms in ethylene (acetylene) to create monosubstituted (R-C-C-H) and symmetrical (R = R') or unsymmetrical (R not equal to R') disubstituted alkynes (R-C-C-R').
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Explanation:
If a large photon strikes the surface, that has enough strength to take out an electrode, which will then travel to the positive side since it is negative. Current is flowing at this stage. Since the reduced photons will be unable to distinguish between atoms, no power can pass.
