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.
One can tell by looking at the titration curve of an acid and base whether the acid used is a strong acid or a weak acid. For a titration of a strong acid and a strong base, the pH at the equivalence point will be neutral, that is, pH 7. If the titration involves a weak acid and a strong base, the pH at the equivalence point will not be neutral, the solution will be basic at the equivalence point.
Answer:
2.82*10^23
Explanation:
please see attached for work!