Give the structures of both 1,2 and 1,4 adducts resulting from reaction of 1 equivalent of hcl with 1,3-pentadiene
1 answer:
1,3-pentadiene has two double bonds which are conjugated, which undergo electrophilic addition reaction on reacting with .
The structure of 1,3-pentadiene is shown in the image.
When strong acid such as reacts with 1,3-pentadiene, the electrophilic addition reaction can occur either on double bond at 1,2-position or at 3,4-position. The reaction that occurs is shown in the image.
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Answer:
<h2>10 m/s²</h2>Explanation:
The acceleration of an object given it's mass and the force acting on it can be found by using the formula
f is the force
m is the mass
From the question we have
We have the final answer as
<h3>10 m/s²</h3>Hope this helps you
Answer : The correct option is, (b) occur when there is more free energy in the reactants than the products.
Explanation :
Endergonic reactions : It i defined as the reaction in which the energy is absorbed during the reaction.
In endergonic reactions, the Gibbs free energy of product is lower than the reactants. That means, ΔG > 0 and the reaction is non-spontaneous.
Exergonic reactions : It i defined as the reaction in which the energy is released during the reaction.
In exergonic reactions, the Gibbs free energy of product is greater than the reactants. That means, ΔG < 0 and the reaction is spontaneous.
Hence, the endergonic reactions is occur when there is more free energy in the reactants than the products.
