Name the following compound: H₂SO₄ *
2 answers:
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Answer:
Esterification reaction
Explanation:
When we have to go from an acid to an ester we can use the <u>esterification reaction</u>. On this reaction, an alcohol reacts with a carboxylic acid on acid medium to produce an ester and water. (See figure).
In this case, we need the <u>methyl ester</u>, therefore we have to choose the <u>appropriate alcohol</u>, so we have to use the <u>methanol</u> as reactive if we have to produce the methyl ester.
Answer:
CH₃CH(CH₃)CH(C₃H₇)CH₂CH(CH₃)₂:
4-isopropyl-2-methylpentane.
Explanation:
Step One: Draw the structure formula of this compound. Parentheses in the formula indicate substitute groups that are connected to the carbon atom to the left.
For example, the first (CH₃) indicates that the second carbon atom from the left is connected to:
- the CH₃- on the left-hand side,
- the -CH(C₃H₇)CH₂CH(CH₃)₂ on the right-hand side,
- a hydrogen atom, and
- an additional CH₃- group that replaced one hydrogen atom.
Each carbon atom in this compound is connected to four other atoms. All bonds between carbon atoms are single bonds.
The C₃H₇ in the second pair of parentheses is the condensed form of CH₃CH₂CH₂-. See the first sketch attached. Groups in parentheses are highlighted.
Step Two: Find the carbon backbone. The backbone of a hydrocarbon is the longest chain of carbon atoms that runs through the compound. See the second sketch attached. The backbone of this compound consists of seven carbon atoms and is highlighted in green. The name for this backbone shall be heptane.
Step Three: Identify and name the substitute groups.
The two substitute groups are circled in blue in the second sketch.
- The one on the right -CH₃ is a methyl group.
- The one on the left is branched.
This group can be formed by removing one hydrogen from the central carbon atom in propane. The name for this group is isopropyl.
Step Four: Number the atoms.
Isopropyl shall be placed before methyl. Start from the right end to minimize the index number on all substitute groups. The methyl group is on carbon number two and the isopropyl group on carbon number four. Hence the name:
4-isopropyl-2-methylheptane.
An individual is hospitalized and the initial blood work indicates high levels of in the blood and a pH of 7. 47. This would indicate the individual probably has compensated respiratory acidosis.
A chronic illness usually leads to compensated respiratory acidosis because the kidneys have time to adjust to the delayed onset. Even if the is elevated in a compensated respiratory acidosis, the pH is within the usual range.
The kidneys counteract a respiratory acidosis by increasing the amount of that tubular cells reabsorb from the tubular fluid, the amount of
that collecting duct cells secrete while also producing
, and the amount of
buffer that is formed through ammoniagenesis.
Respiratory acidosis is frequently brought on by hypoventilation as a result of: breathing depression , paralysis of the respiratory muscles, diseases of the chest wall , abnormalities of the lung parenchyma and abdominal squeezing.
Learn more about Respiratory acidosis here;
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