Answer:
A carboxylate salt and water
Explanation:
A carboxylic acid is an organic compound that has general formula RCOOH, where R is a carbon chain. Because it's an acid, the neutralization will happen when it reacts with a base, such as NaOH.
When this reaction occurs, the base will dissociate in Na⁺ and OH⁻, and the acid will ionize in RCOO⁻ and H⁺, so the products will be RCOO⁻Na⁺ (a carboxylate salt) and H₂O (water).
I believe the answer is option B. The bonded pair of valence electrons are shown using circles
Explanation:
This is correct!
Ions that exist in both the reactant and product side of the equation are referred to as spectator ions. Overall, they do not partake in the reaction. If they are present on both sides of the equation, you can cancel them out.
An example is;
Na+(aq) + Cl−(aq) + Ag+(aq) + NO3−(aq) → Na+(aq) + NO3−(aq) + AgCl(s)
The ions; Na+, NO3−(aq) would be cancelled out to give;
Cl−(aq) + Ag+(aq) → AgCl(s)
Answer: increasing frequency or energy and decreasing wavelength.
Explanation:
Electromagnetic wave is defined as the wave which is associated with both electrical and magnetic component associated with them. They can travel in vacuum as well and travel with the speed of light i.e
The electromagnetic spectra consist of radio waves, microwaves, infrared ,Visible , ultraviolet, X rays and gamma rays arranged in order of increasing frequency or increasing energy and decreasing wavelengths.
Answer:
The three-step synthesis of trans-2-pentene from acetylene is as follows.
<u>Step -1:</u> Formation of higher order terminal alkyne on reaction with sodium acetylides with haloalkanes.
<u>Step -2:</u> Formation terminal alkyne to nonterminal alkynes.
<u>Step -3:</u> Formation of trans-pent - 2-pent-ene by reduction.
Explanation:
Synthesis of trans-pent-2-yne from ethyne takes place is mainly a three step synthesis which involves formation of higher order terminal alkyne on reaction with sodium acetylides with haloalkane. Second step involves the further alkylation of terminal alkynes to higher order nonterminal alkynes and the third step involves the formation of trans-2-ene by dissolving reduction method.
The chemical reaction of each step of chemical reactions is as follows.
