Construct a three-step synthesis of trans-2-pentene from acetylene by dragging the appropriate formulas into the bins. Note that
each bin will hold only one item, and not all of the given reagents or structures will be used. (Me = methyl, CH3; Et = ethyl, CH3CH2.)
1 answer:
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.
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Answer:
Metallic bonding
Explanation:
Metals have low ionization energies. Therefore, their valence electrons are easily delocalized (attracted to the neighbouring metal atoms). These delocalized electrons are then not associated with a specific metal atom. Since the electrons are “free”, the metal atoms have become cations, and the electrons are free to move throughout the whole crystalline structure.
We say that a metal consists of an array of cations immersed in a sea of electrons .
The electrons act as a “glue” holding the cations together.
Metallic bonds are the attractive forces between the metal cations and the sea of electrons.
In an NaK alloy, for example, the Na and K atoms contribute their valence electrons to the "sea". The atoms aren’t bonded to each other, but they are held in place by the metallic bonding.
