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Propan acid Propanon

You are given samples of propanal, 2-propanone, and ethanoic acid. Describe how you would use chemical tests, such as acid—base indicators and oxidizing agents, to distinguish among the three compounds. [Pg.898]

Figure 2. Mechanism for the Formation of 2-Pentenal, Propanal, 2-Propanone and Ethanal from the Thermal Degradation and Retro-Aldol Condensation of Linolenic Acid. Figure 2. Mechanism for the Formation of 2-Pentenal, Propanal, 2-Propanone and Ethanal from the Thermal Degradation and Retro-Aldol Condensation of Linolenic Acid.
Describe the tests that you could do to distinguish between a ethanoic acid and ethanoyl chloride b propanal and propanone. [Pg.83]

Synonyms ACN AI3-01238 BRN 0635680 Caswell No. 004 CCRIS 5953 Chevron acetone Dimethylformaldehyde Dimethyl ketal Dimethyl ketone DMK EINECS 200-662-2 EPA pesticide chemical code 004101 FEMA No. 3326 Ketone propane p Ketopropane Methyl ketone NSC 135802 Propanone Propan-2-one 2-Propanone Pyroacetic acid Pyroacetic ether RCRA waste number U002 Sasetone UN 1090. UN 1091. [Pg.64]

The acid-catalyzed cyclization of 3-(2-hydroxyphenyl)propan-l-ones leads to chrom-2-enes. This reaction accounts for the formation of 2,4-diphenylchrom-2-ene from the reaction of phenylmagnesium bromide on coumarin. The organometallic reagent ring-opens the coumarin to the ketone which cyclizes to the chromene on boiling with acetic acid (Scheme 26) (63T839). In a similar manner, various benzocoumarins afford propanones which cyclize readily in acetic acid to the naphthopyran (70JCS(C)1758). [Pg.763]

The important polymer intermediate bis-phenol A [2,2-bis-(4-hydroxy-phenyI)propane] used, among other things, in epoxy resins, is made by an acid-induced condensation of 2-propanone and benzenol. Write a stepwise mechanism for this reaction that is consistent with the nature of the reactants and the products. [Pg.1340]

Procedure (1) will distinguish ethanoic acid (2) and (3) will distinguish propanal from 2-propanone. [Pg.1091]

Diphenyl-l-propene-3-one gives (depending on the ratio ketone silane acid) 1,3-diphenyl-l-propanone (126) (1 1 10) and 1,3-diphenyl-propane (127) (1 3 10), respectively85. ... [Pg.45]

SYNS ACETON (GERMAN, DUTCH, POLISH) ACETONE OILS pOT) CHEVRON ACETONE DIMETHYLFORMALDEHYDE DIMETHYLKETAL DIMETHYL KETONE FENL No. 3326 KETONE, DIMETHAT KETONE PROPANE P-KETOPROPANE METHAT. KETONE PROPANONE 2-PROPANONE PYROACETIC ACID PYROACETIC ETHER RCRA WASTE NUMBER U002... [Pg.10]

Note that oxidizing 2-propanol yields a ketone, not an aldehyde. Unlike aldehydes, ketones resist further oxidation to carboxylic acids. Thus, while the propanal formed by oxidizing 1-propanol easily oxidizes to form propanoic acid, the 2-propanone formed by oxidizing 2-propanol does not react to form a carboxylic acid. [Pg.759]

Very well studied are arylaliphatic compounds ), especially those which have one double bond. By varying the ratio of carbonyl silane acid, the course of reaction can be immensely influenced. If the ratio is 1 1 10, only the double bond is hydrogenated ) whereas a mixture 1 3 10 hydrogenates both the double bond and the carbonyl function ). When this reducing combination is used in the former ratio, 3-benzoyl-butyric acid yields 4-phenyl-vaIeric acid (722), p.p -dinitrobenzophenone p,p -dinitrodiphenylmethane(123), l,6-diphenyl-hexane-l,6-di-one 1,6-diphenyl-hexane 124) and p-methoxybenzaldehyde p-methoxytoluene (725), respectively ). l,3-Diphenyl-l-propene-3-one gives (depending on the ratio ketone silane acid) 1,3-diphenyl-l-propanone (726) (1 1 10) and 1,3-diphenyI-propane (727) (1 3 10), respectively ). [Pg.45]

CAS 67-64-1 EINECS/ELINCS 200-662-2 UN 1090 (DOT) UN 1091 (DOT) FEMA 3326 Synonyms Acetone oils Dimethyl formaldehyde Dimethylketal Dimethylketone DMK Ketone, dimethyl Ketone propane 3-Ketopropane Methyl ketone Propanone 2-Propanone Pyroacetic acid Pyroacetic ether Classification Aliphatic ketone Empirical CsHsO Formula CHsCOCHs... [Pg.959]

Ketone, dimethyl Ketone propane p-Ketopropane Methyl ketone Propanone 2-Propanone Pyroacetic acid Pyroacetic ether... [Pg.39]

Acetyl propane. See Methyl isopropyl ketone Acetyl 2-propanone. See Acetylacetone Acetylpropionic acid 3-Acetylpropionic acid p-Acetylpropionic acid. See Levulinic acid Acetylpropionyl. See Pentane-2,3-dione Acetyl pyrazine. See 2-Acetyl pyrazine 2-Acetyl py razi ne... [Pg.55]

As shown in Equation 9.6, propanal (CH3CH2CHO) on treatment with peretha-noic acid (peracetic acid, CH3CO3H) produces propanoic (CH3CH2CO2H) and etha-noic (acetic, CH3CO2H) acids, the former the result of oxidation and the latter the result of reduction. Similarly, as shown in Equation 9.7, propanone (acetone [(CH3) 2C=0]) under the same conditions produces methyl ethanoate (methyl acetate, CH3CO2CH3) and ethanoic (acetic, CH3CO2H) acids. [Pg.737]

Synonyms Acetone oils Dimethyl formaldehyde Dimelhylkelal Dimethylketone DMK Ketone, dimethyl Ketone propane P-Ketopropane Methyl ketone Pro-panone 2-Propanone Pyroacelic acid l roacetic ether... [Pg.1960]


See other pages where Propan acid Propanon is mentioned: [Pg.546]    [Pg.329]    [Pg.1017]    [Pg.792]    [Pg.86]    [Pg.542]    [Pg.50]    [Pg.641]    [Pg.64]    [Pg.55]    [Pg.2291]    [Pg.55]    [Pg.59]    [Pg.7]    [Pg.1017]    [Pg.1017]    [Pg.336]    [Pg.38]    [Pg.193]   
See also in sourсe #XX -- [ Pg.94 ]




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Propan acid

Propanone, acidity

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