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Citrus2011 [14]
3 years ago
14

Design a synthesis of 2-chloro-4-nitroanisole from benzene or any mono-substituted benzene. choose the best option for the immed

iate precursor to the target molecule.
Chemistry
2 answers:
Lunna [17]3 years ago
6 0

The reaction starts with Anisole which is ortho-para directing group. So reacting anisole with Con H2SO4 and con HNO3 gives paranitro anisole.

Now paranitro anisole is a meta directing group and having low electron density in meta position which on reacting with Cl2 and anh AlCl3 directs the chlorine to meta position of nitro group and results in formation of the product 2-chloro-4-nitroanisole.

Thus, the product is 2-chloro-4-nitroanisole

liberstina [14]3 years ago
3 0

The response begins with Anisole which is ortho-para coordinating gathering. So responding anisole with Con H2SO4 and con HNO3 gives paranitro anisole.  

Further Explanation:  

Presently paranitro anisole is a meta coordinating gathering and having low electron thickness in meta position which on responding with Cl2 and anh AlCl3 guides the chlorine to meta position of nitro gathering and results in development of the item 2-chloro-4-nitroanisole. Subsequently, the item is 2-chloro-4-nitroanisole.  

Mono substituted benzene:  

A particle or practical gathering where just a single hydrogen has been supplanted by another molecule or gathering. These substituents are not restricted to methyl bunches as appeared here. When thinking about alkene strength, just carbon substituents matter (i.e., - CH3 or - Ph matter however - Br or - OCH3 don't). Benzene.  

Mono substituted Benzene Derivatives:  

For those substituent bunches which are named distinctly with prefixes, frequently the prefix is connected to the parent name in the manner we have turned out to be utilized to.  In the event that the benzene ring is on a carbon bind which is utilized to shape the root name, at that point the benzene ring utilizes the prefix: phenyl.

Subject: chemistry

Level: college

Keywords: Mono substituted benzene, Mono substituted Benzene Derivatives.

Related links:  

Learn more about evolution on

brainly.com/question/1566156

brainly.com/question/5354719

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How many grams of hydrogen are contained in 2.00 mol of C6H7N
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Answer:- 14.0 moles of hydrogen present in 2.00 moles of [tex]C_6H_7N .

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Need help asap with this chemistry if someone could help me
Burka [1]

Answer:

<h3>1)</h3>

Structure One:

  • N: -2
  • C: 0
  • O: +1

Structure Two:

  • N: 0
  • C: 0
  • O: -1

Structure Three:

  • N: -1
  • C: 0
  • O: 0.

Structure Number Two would likely be the most stable structure.

<h3>2)</h3>
  • All five C atoms: 0
  • All six H atoms to C: 0
  • N atom: +1.

The N atom is the one that is "likely" to be attracted to an anion. See explanation.

Explanation:

When calculating the formal charge for an atom, the assumption is that electrons in a chemical bond are shared equally between the two bonding atoms. The formula for the formal charge of an atom can be written as:

\text{Formal Charge} \\ = \text{Number of Valence Electrons in Element} \\ \phantom{=}-\text{Number of Chemical Bonds} \\\phantom{=} - \text{Number of nonbonding Lone Pair Electrons}.

For example, for the N atom in structure one of the first question,

  • N is in IUPAC group 15. There are 15 - 10 = 5 valence electrons on N.
  • This N atom is connected to only 1 chemical bond.
  • There are three pairs, or 6 electrons that aren't in a chemical bond.

The formal charge of this N atom will be 5 - 1 - 6 = -2.

Apply this rule to the other atoms. Note that a double bond counts as two bonds while a triple bond counts as three.

<h3>1)</h3>

Structure One:

  • N: -2
  • C: 0
  • O: +1

Structure Two:

  • N: 0
  • C: 0
  • O: -1

Structure Three:

  • N: -1
  • C: 0
  • O: 0.

In general, the formal charge on all atoms in a molecule or an ion shall be as close to zero as possible. That rules out Structure number one.

Additionally, if there is a negative charge on one of the atoms, that atom shall preferably be the most electronegative one in the entire molecule. O is more electronegative than N. Structure two will likely be favored over structure three.

<h3>2)</h3>

Similarly,

  • All five C atoms: 0
  • All six H atoms to C: 0
  • N atom: +1.

Assuming that electrons in a chemical bond are shared equally (which is likely not the case,) the nitrogen atom in this molecule will carry a positive charge. By that assumption, it would attract an anion.

Note that in reality this assumption seldom holds. In this ion, the N-H bond is highly polarized such that the partial positive charge is mostly located on the H atom bonded to the N atom. This example shows how the formal charge assumption might give misleading information. However, for the sake of this particular problem, the N atom is the one that is "likely" to be attracted to an anion.

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