Answer: Option (C) is the correct answer.
Explanation:
Chemical formula of a secondary amide is R'-CONH-R, where R and R' can be same of different alkyl or aryl groups. Here, the hydrogen atom of amide is attached to more electronegative oxygen atom of the C=O group.
Therefore, the hydrogen atom will be more strongly held by the electronegative oxygen atom. As a result, there will be strongly hydrogen bonded in the liquid phase of secondary amide.
Whereas chemical formula of nitriles is RCN, ester is RCOOR' and acid chlorides are RCOCl. As no hydrogen bonding occurs in any of these compounds because hydrogen atom is not being attached to an electronegative atom.
Thus, we can conclude that secondary amides are strongly hydrogen bonded in the liquid phase.
Answer: The statement (B) is not true about chemical reactions.
Explanation:
A chemical reaction rate is affected by the several factors few of which are temperature, concentration of reactants, surface area etc.
In a chemical reaction, if temperature is increased then the rate of reaction will increase because it will increase the average kinetic energy of the reactant molecules. Thus, large number of molecules will have minimum energy required for an effective collision.
It is known that increasing the amount of reactants will increase the rate of reaction.
Therefore, rate of reaction will change if concentration or temperature is changed.
Hence, the statement (B) is not true about chemical reactions.
Answer:
It is based on testable and replicable evidence.
Answer:
A. H3O+/OH−
Explanation:
A conjugate acid-base pair are a pair of molecules that differ in 1 H⁺
A. The conjugate pair of H₃O⁺ = H₂O not OH⁻
B. The conjugate pair of NH₄⁺ is NH₃
C. The conjugate pair of C₂H₃O₂⁻ is HC₂H₃O₂
D. The conjugate pair of H₂SO₃ is HSO₃⁻
That means right option, that is not a conjugate acid-base pair, is:
<h3>A. H3O+/OH−
</h3>
Solution:
After the reaction of mixture is worked-up Washing three times the organic with sodium carbonate helps to decrease the solubility of the organic layer into the aqueous layer. This allows the organic layer to be separated more easily.
And then the reaction washed by saturated NACL we have The bulk of the water can often be removed by shaking or "washing" the organic layer with saturated aqueous sodium chloride (otherwise known as brine). The salt water works to pull the water from the organic layer to the water layer.
