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Tems11 [23]
3 years ago
15

A _____________reaction mechanism involves loss of a leaving group, formation of a ________ followed by the removal of a proton

(H ) from the adjacent Carbon.
A. electrophile
B. carbocation
C. E1
D. E2
E. nucleophile
Chemistry
1 answer:
Molodets [167]3 years ago
7 0

Answer:

The correct answer is Option C (E1) and Option B (carbocation).

Explanation:

  • Intramolecular immunity idols are considered as that of the formation mechanism with E1 responses or reactivity.
  • Reactants with E1 were indeed obligations of both parties, meaning that an E1 reaction was conducted thru all the two stages known as ionization but rather deprotonation. Involves the absence of either an aromatic ring, a carbocation has been generated throughout the ionization solution.

Some other possibilities offered aren't relevant to the procedure outlined. So the above alternative is accurate.

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Answer:

The electronic configuration that are incorrectly written is 1s²2s³2p⁶, 4s²3d¹⁰4p⁷, 3s¹ and 2s²2p⁴.

Explanation:

The electronic configuration of the elements corresponds to how all the electrons of an element are arranged in energy levels and sub-levels.

There are 7 energy levels —from 1 to 7— whose sublevels are described as s, p, d and f.

All electronic configurations begin with the term "1s" —corresponding to the sublevel s of level 1— so 4s²3d¹⁰4p⁷, 3s¹ and 2s²2p⁴ are incorrectly written. In addition, 4s²3d¹⁰4p⁷ is written incorrectly because is impossible to jump from the sublevel "s" to the sublevel "d" —which is found from level 3 and up— without passing through the sublevel "p".

In the case of 1s²2s³2p⁶, the wrong thing is that the sublevel "s" can only hold two electrons, not three.

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