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Heterocíclos - ¿Verdadero o Falso?

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Heterocíclos - ¿Verdadero o Falso?

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Serie de Verdadero o Falso sobre Heterocíclos, primer tema de química orgánica 2.

Created by

Juan Ignacio
Juan Ignacio
Uruguay

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Heterocíclos - ¿Verdadero o Falso?
 

Heterocíclos - ¿Verdadero o Falso?Online version

Serie de Verdadero o Falso sobre Heterocíclos, primer tema de química orgánica 2.

by Juan Ignacio
1

La piridina pierde aromaticidad cuando se protona en el nitrógeno.

2

En el furano, la SEAr ocurre mayoritariamente en C-2

3

La reacción de Chichibabin introduce un grupo amino en C3 de la piridina

4

En la piridina, las posiciones más reactivas para la SNAr son C-2 y C-4

5

El pirrol es más básico que la piridina porque el par de electrones del nitrógeno no participa en la aromaticidad.

6

El tiofeno puede sufrir halogenación en presencia de catalizadores de Lewis

7

El furano es más reactivo que el tiofeno en SEAr

8

En la piridina, el par libre de electrones del nitrógeno no forma parte del sistema aromático

9

La reducción catalítica de la piridina con hidrógeno produce piperidina

 
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