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What Are Alcohols

Alcohol A compound containing an —OH (hydroxyl) group bonded to an sp hybridized carbon. [Pg.240]

Methanol, CH3OH. (a) Lewis structure and (b) ball-and-stick model.The measured H — 0 — C bond angle in methanol is 108.6°, very close to the tetrahedral angle of 109.5°. [Pg.240]

We derive the lUPAC names for alcohols in the same manner as those for alkanes, with the exception that the ending of the parent alkane is changed from -e to -oL The ending -ol tells [Pg.240]

Select, as the parent alkane, the longest chain of carbon atoms that contains the —OH, and number that chain from the end closer to the —OH group. In numbering the parent chain, the location of the —OH group takes precedence over alkyl groups and halogens. [Pg.240]

Change the suffix of the parent alkane from -e to -ol (Section 3.5), and use a number to show the location of the —OH group. For cyclic alcohols, numbering begins at the carbon bearing the —OH group. [Pg.240]


A (a) What are alcohols and phenols (b) How do they differ (c) Why can alcohols and phenols be viewed as derivatives of hydrocarbons as derivatives of water ... [Pg.946]

What are some of the alternatives for this procedure Well, one can use NaOH (lye) in place of KOH but the yields will go down. Also, what about using denatured alcohol instead of pure ethanol Denatured alcohol is ethanol contaminated with 5-10% methanol. The methanol is there because it is poisonous and prevents people from using the ethanol for drinking. This means that places like the giant hardware stores can carry gallons of cheap contaminated ethanol as many of you have discovered. This product CAN be used. [Pg.40]

Hydroboration-oxidation of 1,4-di-f-butylcyclohexene gave three alcohols 9-A (77%), 9-B (20%), and 9-C (3%). Oxidation of 9-A gave a ketone 9-D that was readily converted by either acid or base to an isomeric ketone 9-E. Ketone 9-E was the only oxidation product of alcohols 9-B and 9-C. What are the structures of compounds 9A-9E ... [Pg.360]

What are the products of oxidation and reduction of the monosaccharides Mucic add, of which the preparation from d-galactose has been described, is optically inactive and incapable of resolution, just like duldtol, the corresponding hexahydric alcohol. As the formula shows, the four asymmetric carbon atoms of galactose form two pairs (2, 5 and 3, 4) having the same substituents but opposite arrangement in space, and when the carbon atoms 1 and 6 become alike, inactive forms are produced by intramolecular compensation, as in mesotartaric acid. [Pg.399]

A. It is confusing because the term is often used to refer to various preparations derived from Salvia. Technically, in pharmacy and medicine the dictionary definition of an extract is a solid preparation obtained by evaporating a solution of a drug. There is also such a thing as a fluid extract (or tincture), which is a concentrated liquid preparation containing a definite proportion of the active principles of a medicinal substance. The solvent usually used is ethyl alcohol or a mixture of ethyl alcohol and water. However various Salvia preparations are often referred to (loosely) as extracts. Q. What are the advantages of using extracts . [Pg.47]

H. Berger (Koninklijke/Shell Laboratorium, Amsterdam) Concerning the effect of cyanides on metal catalysis (deactivation and formation of oxygenated products), what are your arguments against the explanation that the metal ion becomes completely inactive, while the products arise from a mechanism analogous to that proposed by Berger [Rec. Trav. Chim. 82, 733 (1963)] for the oxidation in tert-butyl alcohol with excess mercaptan relative to base, Did you check that no hydrolysis of disulfide occurs in the presence of cyanide ... [Pg.193]

Now the influence of water or ammonia on copper catalysts is being investigated. Previously A. BAIKER and coll, have shown that ammonia could modify the catalytic properties of copper catalysts used in the amination of alcohols (9). These authors noticed the formation of copper nitride after NH3 exposure at a temperature of about 300°C which is the reaction temperature of our study. The first results that we obtained in our study showed that both H2O and NH3 decrease significantly the copper dispersion in unpromoted catalysts and that this modification is less significant when Ca or Mn are added to the Cu-Cr catalyst. We are now studying what are the superfical modifications consecutive to the addition of promoters or/and water and ammonia. [Pg.349]

Exercise 15-23 What are the expected products on heating the following alcohols with strong sulfuric acid Give your reasoning. [Pg.632]

What are the products when deuterium labeled alcohol is reacted with NAD in tlie presence of alcohol dehydrogenase as shown below ... [Pg.107]

Methadone is an odorless, white powder that dissolves easily in water and alcohol. In methadone treatment programs, it is often mixed with an insoluble matrix to form what are known as methadone biscuits. These biscuits stay in the stomach longer because it takes awhile for the stomach acids to break down the matrix. This is important because it allows more of the methadone to be absorbed, rather than passing quickly through the stomach when in liquid form. [Pg.324]

Several approaches to what are formally Si-0 and O-Si-O heterocycles have been reported, although these reactions invariably involve the use of the Si-O bond only as a temporary tether. The coupling and RCM of dissymmetric alcohols was reported by Eustache and co-workers <01TL239> and this method was applied in the synthesis of attenol A <020L4105>. Denmark and Yang performed the RCM of Si-O tethered dienes in tandem with silicon-assisted cross-... [Pg.22]

What are the products of treatment of perfluorocyclopentene with potassium hydroxide in tert-butyl alcohol (compound G), and in diglyme (compound H) ... [Pg.16]

Question What are the names of the compounds obtained when the carbonyl group of D-fructose is reduced to an alcohol ... [Pg.40]

What are the alcohol structures and functional group isomers of diethyl ether, C4H10O or C2H5 O C2H5 ... [Pg.51]

Question 4.15 Three routes for the synthesis of alkoxides involve (i) the reaction of LnCb with an alkali metal alkoxide, (ii) reaction of an alkali metal with an alcohol, (iii) the reaction of a silylamide [Ln N(SiMe3)2 3] with an alcohol. What are the advantages and disadvantages of each ... [Pg.60]


See other pages where What Are Alcohols is mentioned: [Pg.1100]    [Pg.1100]    [Pg.517]    [Pg.239]    [Pg.240]    [Pg.241]    [Pg.243]    [Pg.245]    [Pg.272]    [Pg.1100]    [Pg.1100]    [Pg.517]    [Pg.239]    [Pg.240]    [Pg.241]    [Pg.243]    [Pg.245]    [Pg.272]    [Pg.226]    [Pg.178]    [Pg.562]    [Pg.396]    [Pg.206]    [Pg.82]    [Pg.7]    [Pg.163]    [Pg.340]    [Pg.365]    [Pg.159]    [Pg.783]    [Pg.198]    [Pg.115]    [Pg.1131]    [Pg.985]    [Pg.10]    [Pg.10]    [Pg.132]    [Pg.263]    [Pg.198]    [Pg.327]    [Pg.354]    [Pg.305]   


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