Answer:
[H+] = 1.74 x 10⁻⁵
Explanation:
By definition pH = -log [H+]
Therefore, given the pH, all we have to do is solve algebraically for [H+] :
[H+] = antilog ( -pH ) = 10^-4.76 = 1.74 x 10⁻⁵
Answer:
enantiomers
Explanation:
L and D stand for levorotatory and dextrorotatory respectively. A levorotatory molecule will rotate the plane of plane polarised light left and a dextrorotatory molecule will rotate the plane of plane polarised light right. L and D molecules are non superimposable mirror image of each other. Therefore they are also known as enantiomers.
Answer:
option C= hydrolysis and break down
Explanation:
All other three pairs are correct coupling of each others.
Option A= dehydration synthesis and hydrolysis
Dehydration synthesis:
In dehydration synthesis monomers combine through the covalent bonds and form large molecules. The large molecules are called polymers. The water as a byproduct also released when monomers joints together.
Hydrolysis:
In hydrolysis the polymers are break down into monomers by using water molecules. The catalysts are also required in this process.
Option B= Catabolic and Anabolic
Anabolic:
In this process smaller molecules combine to gather to form large complex molecules by using energy.
For example simple glucose molecules join together to form large disaccharides.
Catabolic:
It is the break down of large complex molecules to the smaller molecules.
For example during cellular respiration sugar molecules break down and generate energy.
Option D= Break down and synthesis
The break down and synthesis are also reverse pair of each others. The synthesis involve the formation of molecules form smaller component while the break down involve destruction of molecules into smaller units.
2nd law i think
Have a good evening and im sorry if im wrong
Bai sisters
Answer:
Azide synthesis is the first method on the table of synthesis of primary amines. The Lewis structure of the azide ion, N3−, is as shown below.
an azide ion
An “imide” is a compound in which an N−−H group is attached to two carbonyl groups; that is,
imide linkage
You should note the commonly used trivial names of the following compounds.
phthalic acid, phthalic anhydride, and phthalimide
The phthalimide alkylation mentioned in the reading is also known as the Gabriel synthesis.
If necessary, review the reduction of nitriles (Section 20.7) and the reduction of amides (Section 21.7).
Before you read the section on reductive amination you may wish to remind yourself of the structure of an imine (see Section 19.8).
The Hofmann rearrangement is usually called the Hofmann degradation. In a true rearrangement reaction, no atoms are lost or gained; however, in this particular reaction one atom of carbon and one atom of oxygen are lost from the amide starting material, thus the term “rearrangement” is not really appropriate. There is a rearrangement step in the overall degradation process, however: this is the step in which the alkyl group of the acyl nitrene migrates from carbon to nitrogen to produce an isocyanate.
Explanation:
