Sulfuric acid is prepared industrially by means of the response of water with sulfur trioxide which in turn is made by way of a chemical combination of sulfur dioxide and oxygen both by way of the touch system or the chamber system.
H2SO4 (l) H2O (g) + SO3 (g).
The reaction is highly exothermic as an enormous amount of heat is liberated.
The usual approach is to dilute the sulfur trioxide in sulphuric acid. This produces oleum. SO3 (g) + H2SO4 → H2S2O7 (1) Oleum can be in addition diluted in water to acquire concentrated sulphuric acid.
An acid catalyst is added to protonate the carbonyl carbon. How does this catalyze the response, robust acid catalysts catalyze the hydrolysis and transesterification of esters which enables the mechanism with a view to boom the electrophilicity of the carbonyl carbon to assist protonate the carbonyl oxygen.
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Answer:
The answer to your question is organic or non polar compound.
Explanation:
Acetone is an organic compound then it's organic and one characteristic of these compounds is that they are non polar.
Water, aqueous hydrochloric acid and aqueous sodium chloride are inorganic and they are polar, they dissolve compounds similar to them, inorganic and polar compounds.
Plants most commonly break large rock into smaller pieces by having the plant root grow into cracks in rocks. The plant root from below the surface grows and that's how they break rocks into pieces.
Answer:
2-methyl-2-pentanol is produced as a major product
Explanation:
- Double bond in 2-methyl-2-pentene is protonated first by consuming a proton from
. - A carbocation intermediate is formed after protonation of double bond. Most stable carbocation is formed as a major intermediate.
- Here a tertiary carbocation is formed as a major intermediate.
gives subsequent nucleophilic addition to the carbocation intermediate and produce 2-methyl-2-pentanol as a major product.- Reaction mechanism and major organic product has been shown below.
