Answer:
A. Methanol
B. 2-chloropropan-1-ol
C. 2,2-dichloroethanol
D. 2,2-difluoropropan-1-ol
Explanation:
Primary alcohols are stronger acids than secondary alcohols which are stronger than tertiary alcohols.
This trend is so because of the stability of the alkoxide ion formed(stabilising the base, increases the acidity). A more stabilised alkoxide ion is a weaker conjugate base (dissociation of an acid in water).
By electronic factors, When there are alkyl groups donating electrons, the density of electrons on th O- will increase a d thereby make it less stable.
By stearic factors, More alkyl group bonded to the -OH would mean the bulkier the alkoxide ion which would be harder to stabilise.
Down the group of the periodic table, basicity (metallic character) decreases as we go from F– to Cl– to Br– to I– because that negative charge is being spread out over a larger volume that is electronegativity decreases down the group.
Electronegative atoms give rise to inductive effect and a decrease in indutive effects leads to a decrease in acidity. Therefore an Increasing distance from the -OH group lsads to a decrease in acidity.
From above,
A. Methanol
B. 2-chloropropan-1-ol
C. 2,2-dichloroethanol
D. 2,2-difluoropropan-1-ol
Answer:
Explanation:
we know that 1 km =1000 m and 1 hour =60 min
therefore
239 km/hr =239*1000m/60 min=3983.3 m/min
Answer:
There’s a high need for energy storage and are very expensive. Renewable energy is also not always available because some need sun while others need wind.
Explanation:
Answer:
The hydrolysis in aqueous HCl of compound A can lead to the formation of a carboxylic acid and an alcohol.
Explanation:
The picture shows the structures of compound A, benzoncaine and the possible products of the proposed reaction.
The acidic hydrolysis is the inverse of the esterification reaction. Therefore, the ester group of compund A will react to form the equivalent carboxylic acid and alcohol.
In order to form benzocaine, the hydrolysis happens in with the nitrile group.
Answer:
hydrate
Explanation:
when a hydrate is heated,it changes color due to the exothermic reaction taking place.the structure of the complex changes but not entirely.this result in the sample to to not dissolve completely and we can observe the small traces of the sample.
