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Heterociclos aromáticos

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Heterociclos aromáticos

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Verdadero o falso sobre el tema de heterociclos aromáticos

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Nico 826
Nico 826
Uruguay

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Heterociclos aromáticos
 

Heterociclos aromáticosOnline version

Verdadero o falso sobre el tema de heterociclos aromáticos

by Nico 826
1

En el pirrol, el par de electrones libres del nitrógeno participa en la aromaticidad del anillo.

2

En la piridina, el nitrógeno aporta su par de electrones libres al sistema aromático.

3

La piridina es mas básica que la piperidina debido a que el par de electrones libres del nitrógeno en la piridina está en hibridación sp2 y el par de electrones libres del nitrógeno de la piperidina está en hibridación sp3

4

La piridina y el benceno presentan reactividad similar en sustituciones electrofílicas aromáticas.

5

El pirrol es más reactivo que el benceno en sustituciones electrofílicas aromáticas.

6

En la piridina, la sustitución nucleofílica aromática ocurre preferentemente en las posiciones C3 y C5.

7

Los N-óxidos tienen velocidades de reacción en sustituciones nucleofílicas mas lentas que la Piridina

 
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