Answer:
fitness. the ability of an organism to survive and reproduce in its environment. adaptation. the inherited characteristic that increases an organism's chance of survival.
A carboxylic acid is named in the IUPAC system by replacing the -e in the name of the parent alkane with -<u>oic acid</u>
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<h3>What is carboxylic acid?</h3>
Carboxylic acid is an organic acid that contains a carboxyl group (C(=O)OH) attached to an R-group. The general formula of a carboxylic acid is R−COOH or R−CO2H, with R referring to the alkyl, alkenyl, aryl, or other group. Carboxylic acids occur widely. Important examples include the amino acids and fatty acids. Deprotonation of a carboxylic acid gives a carboxylate anion.
Carboxylic acids are commonly identified by their trivial names. They often have the suffix -ic acid. IUPAC-recommended names also exist; in this system, carboxylic acids have an -oic acid suffix. For example, butyric acid (C3H7CO2H) is butanoic acid by IUPAC guidelines. For nomenclature of complex molecules containing a carboxylic acid, the carboxyl can be considered position one of the parent chain even if there are other substituents, such as 3-chloropropanoic acid. Alternately, it can be named as a "carboxy" or "carboxylic acid" substituent on another parent structure, such as 2-carboxyfuran.
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Answer:
A mixture of 100. mL of 0.1 M HC3H5O3 and 50. mL of NaOH
Explanation:
The pH of a buffer solution is calculated using following relation
Thus the pH of buffer solution will be near to the pKa of the acid used in making the buffer solution.
The pKa value of HC₃H₅O₃ acid is more closer to required pH = 4 than CH₃NH₃⁺ acid.
pKa = -log [Ka]
For HC₃H₅O₃
pKa = 3.1
For CH₃NH₃⁺
pKa = 10.64
pKb = 14-10.64 = 3.36 [Thus the pKb of this acid is also near to required pH value)
A mixture of 100. mL of 0.1 M HC3H5O3 and 50. mL of NaOH
Half of the acid will get neutralized by the given base and thus will result in equal concentration of both the weak acid and the salt making the pH just equal to the pKa value.
D is the answer I believe.
Answer:
The answer for 2-hexene is that the structure should have 6 carbon with a double bond beginning on the 2nd carbon atom.
The answer for 1-pentyne is that the structure should have 5 carbon with triple bond beginning on the 1st carbon atom.
Explanation:
<u>2-Hexene</u>
The structural formula for 2-hexene will have 6 carbons because the nomenclature has a -hex prefix, which stands for 6 carbons.
The -ene suffix of the nomenclature means that the organic compound is an alkene. Alkenes are hydrocarbons that contain double covalent bond and have the suffix -ene.
The double bond is on the 2 carbon atom because the nomenclature states that the double bond will be on the 2 carbon atom.
<u>1-Pentyne</u>
The structure will have 5 carbons since the -pent prefix means 5 carbons.
The structure has a triple bond because the -yne suffix means that the structure is an alkyne. An alkyne is a hydrocarbon with triple covalent bonds.
Also, the position of the triple bond is known because the nomenclature of the alkyne states that the triple bond is on the 1st carbon.
