The given
ketone when reacted with base gave
enolate, the enolate formed due to loss of
methylene proton next to carbonyl group. Enolate when treated with
methyle Bromide gave
alpha substituted product.
Strong absorption around 1713 cm⁻¹ in IR spectrum confirms the presence of
Carbonyl group.
The product along with
¹H-NMR values is given below,
The statement that is not true about the exothermic reaction is that the potential energy of the product is higher than the potential energy of the reactant. That is option D.
<h3>What is an exothermic reaction?</h3>
An exothermic reaction is the reaction that releases heat to the environment which causes increase in the immediate environment.
The characteristics of exothermic reaction include the following:
- Activation energy of the forward reaction is smaller than the activation energy of the reverse reaction.
- Heat is released to the environment during reaction.
Since there is release of heat, the product will have a lower energy than the reactant.
Therefore, the statement that is not true about the exothermic reaction is that the potential energy of the product is higher than the potential energy of the reactant.
Learn more about exothermic reaction here:
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<span>Permeable means that a material is full of tiny, connected airspaces that allows water to seep through it.</span>
Answer:
D. Hydrogen bonds between complementary base pairs89
Explanation:
A DNA molecule is composed of two long polynucleotide chains made of four types of nucleotide subunits, two purines (adenine and guanine) and two pyrimidines (cytosine and thymine). These nucleotides are joined by covalent bonds forming a phosphate-sugar backbone. <em>These strands are held to one another with hydrogen bonds between the base portions of complementary nucleotides.</em>
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