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Chimica organica - reazioni generali aldeidi e chetoni Pag. 1
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Estratto del documento

Reazioni di Aldeidi e Chetoni

OH+O H2O → CH3CH(OH)CH2CH2C(OH)CH3 (idratazione)

H2O2 → OH- + H+

CH3CH(OH)CH2CH2C(OH)CH3 → CH3CH(OH)CH2CH2C(OCH3)CH3 (sintesi semiacetali)

H2O3 → OH-

H+ + OH- → H2O

CH3CH(OH)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi acetali)

H2O3 → OH-

H+ + OH- → H2O

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + H2S → CH3CH(OCH3)CH2CH2C(SH)CH3 (sintesi tioacetali)

CH3CH(OCH3)CH2CH2C(SH)CH3 → CH3CH(OCH3)CH2CH2C(SCH3)CH3 (sintesi tioacetali)

H2O3 → OH-

H+ + OH- → H2O

pH 10

C6H5CN + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → C6H5C(CH3)2CH2CH2C(OCH3)CH3 (sintesi cianidrine)

C6H5C(CH3)2CH2CH2C(OCH3)CH3 → C6H5C(CH3)2CH2CH2C(NH2)CH3 (sintesi di immine)

C6H5C(CH3)2CH2CH2C(NH2)CH3 + H2O → C6H5C(CH3)2CH2CH2C(NH2)CH3 (sintesi di immine)

C6H5C(CH3)2CH2CH2C(NH2)CH3 → C6H5C(CH3)2CH2CH2C(NH2)CH3 (sintesi di immine)

C6H5C(CH3)2CH2CH2C(NH2)CH3 + H2O → C6H5C(CH3)2CH2CH2C(NH2)CH3 (sintesi di immine)

C6H5C(CH3)2CH2CH2C(NH2)CH3 + H2O → C6H5C(CH3)2CH2CH2C(NH2)CH3 (sintesi di immine)

CH3CH(OH)CH2CH2C(OH)CH3 + CH3MgBr → CH3CH(OH)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OH)CH2CH2C(OCH3)CH3 + CH3CH(OH)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3CH(OCH3)CH2CH2C(OCH3)CH3 → CH3CH(OCH3)CH2CH2C(OCH3)CH3 (sintesi alcoli superiori)

CH3CH(OCH3)CH2CH2C(OCH3)CH3 + CH3

Dettagli
Publisher
A.A. 2012-2013
2 pagine
SSD Scienze chimiche CHIM/06 Chimica organica

I contenuti di questa pagina costituiscono rielaborazioni personali del Publisher Moses di informazioni apprese con la frequenza delle lezioni di Chimica organica e studio autonomo di eventuali libri di riferimento in preparazione dell'esame finale o della tesi. Non devono intendersi come materiale ufficiale dell'università Università degli Studi di Messina o del prof Romeo Giovanni.