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Izomeria compusilor organici

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Izomeri optici cu doi atomi de carbon<br />

asimetrici cu substituenŃi diferiŃi<br />

2,3,4 trihidroxibutanal<br />

HOH2CCHO Forme eritro si treo<br />

OH<br />

H OH<br />

H<br />

forma eritro<br />

H<br />

H<br />

H<br />

H<br />

I II III IV<br />

CHO<br />

OH<br />

OH<br />

CH 2OH<br />

CHO<br />

HO H<br />

HO H<br />

CH 2OH<br />

H<br />

HO<br />

CHO<br />

OH<br />

H<br />

CH2OH CHO<br />

HO H<br />

H OH<br />

CH 2OH<br />

eritroza treoza<br />

2R, 3R 2S,3S 2R,3S 2S,3R<br />

CHO<br />

OH<br />

OH<br />

CH 2OH<br />

CHO<br />

HO H<br />

H OH<br />

CH 2OH<br />

I şi II sunt enantiomeri (eritro) I + II în părŃi egale = racemic<br />

III şi IV sunt enantiomeri (treo) III + IV în părŃi egale = racemic<br />

I şi II faŃă de III şi IV sunt diastereoizomeri<br />

H<br />

H<br />

CHO CH2OH C<br />

C<br />

H OH<br />

OH<br />

forma eritro<br />

CHO CH2OH C<br />

C<br />

H OH<br />

OH<br />

forma treo<br />

HOH CHO<br />

2C<br />

HOH<br />

CHO<br />

2C<br />

OH<br />

H OH<br />

H<br />

proiectie Newman<br />

HOH<br />

CHO<br />

2C<br />

H<br />

HO<br />

H<br />

OH<br />

proiectie Newman<br />

H<br />

H OH<br />

HO<br />

forma treo

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