Este tipo de isomería se evidencia cuando los compuestos que presentan la misma fórmula empírica, poseen diferencias en la posición de su grupo funcional sobre el esqueleto carbonado.
Por ejemplo: el C9H18 es un alqueno que posee 4 isómeros de posición:
CH2=CH-CH2-CH2-CH2-CH2-CH2-CH2-CH3
1-noneno
CH3-CH=CH-CH2-CH2-CH2-CH2-CH2-CH3
2-noneno
CH3-CH2-CH=CH-CH2-CH2-CH2-CH2-CH3
3-noneno
CH3-CH2-CH2-CH=CH-CH2-CH2-CH2-CH3
4-noneno
En este ejemplo se observa como el doble enlace se va rotando hasta que ya no es posible obtener más isómeros.
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