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.
Answer:
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Answer:
The ionization equation is
⇄
(1)
Explanation:
The ionization equation is
⇄ (1)
As the Bronsted definition sais, an acid is a substance with the ability to give protons thus, H2PO4 is the acid and HPO42- is the conjugate base.
The Ka expression is the ratio between the concentration of products and reactants of the equilibrium reaction so,
![Ka = \frac{[HPO_{4}^{-2}] [H_{3}O^{+}]}{[H_{2}PO_{4}^{-}] [H_{2}O]} = 6.2x10^{-8}](https://tex.z-dn.net/?f=Ka%20%3D%20%5Cfrac%7B%5BHPO_%7B4%7D%5E%7B-2%7D%5D%20%5BH_%7B3%7DO%5E%7B%2B%7D%5D%7D%7B%5BH_%7B2%7DPO_%7B4%7D%5E%7B-%7D%5D%20%5BH_%7B2%7DO%5D%7D%20%3D%206.2x10%5E%7B-8%7D)
The pKa is
The pKa of H2CO3 is 6,35, thus this a stronger acid than H2PO4. The higher the pKa of an acid greater the capacity to donate protons.
In the body H2CO3 is a more optimal buffer for regulating pH due to the combination of the two acid-base equilibriums and the two pKa.
If the urine is acidified, according to Le Chatlier's Principle the equilibrium (1) moves to the left neutralizing the excess proton concentration.
Answer:
Hydrochloric acid reacts with the materials to produce bubbling, or fizzing, a gas, and heat.
Explanation:
Answer:
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