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Group A molecules

Homotopic Groups Not distinguishable under any conditions, chiral or achiral. To have homotopic groups, a molecule must have a finite axis of rotation. Thus the only molecules which cannot have homotopic groups are those whose point groups are Ci, CS) Q, and CCXJV. [Pg.9]

Answer A chiral center, or chiral carbon, is a carbon atom that is bonded to four different groups. A molecule with a single chiral center has two enantiomers, designated D and L (or in the RS system, S and) ). In isoproterenol, only one carbon (asterisk) has four different groups around it this is the chiral center ... [Pg.5]

In fact, the mechanism can occur, but oh ith the best leaving group—a molecule of gaseous nitrogen—as weshattsee later. [Pg.590]

According to the theory, the initial reaction is the formation of an alk-oxide (I) between the base and the sugar hydroxyl group vicinal to the carbonyl group. A molecule of base is then eliminated, to give the free, methylenic intermediate (II). The latter isomerizes to the epoxy compound (III) and thence to the a-dicarbonyl intermediate (IV). Finally, a benzilic acid type of rearrangement, with hydration and dismutation, gives the saccharinic acid. [Pg.64]

The TOCSY experiment allows the generation of cross peaks between virtually all spins in the same spin system. A spin system is a group of spins that all couple to one or more other members of the group. A molecule may contain one spin system, or it may contain a hundred spin systems. There can be no coupling between spins from two different spin systems if there is a nonzero coupling between two spins then those two spins are part of the same spin system. [Pg.121]

The catalyst we will use Is the amino acid L-proline—no derivatization or protection required. It was actually back in 1971 that it was first noted that L-proline will catalyse asymmetric aldols, but until the year 2000 examples were limited to this one cyclization. Treatment of a triketone with proline leads to selective cyclization onto one of the two enantiotopic carbonyl groups. A molecule of proline must condense with the least hindered ketone, and in this case an enamine (rather than an iminium ion) can form. The chiral enamine can select to react with only one of the two other carbonyl groups, and it turns out that it chooses with rather high selectivity the one coloured green in the scheme below. Cyclization, in the manner of a Robinson annelation, and hydrolysis of the resulting iminium ion follow on, releasing the molecule of L-proline to start another catalytic cycle. The isolated product is the bicyclic ketone, in 93% ee. [Pg.1131]

How do we find what point group a molecule belongs to One way is to find all the symmetry elements and then compeu e with the above list of groups. A more systematic procedure is given in Fig. 12.16 [J. B. Calvert,A/n./. Phys.,31,659 (1963)].This procedure is based on the four divisions of point groups. [Pg.360]

Acetic acid (acidum aceticum) with lUPAC name ethanoic acid is used as an everyday food additive. Citric acid, which is also a natural product, is a polyfunc-tional compound with three carboxylic and one OH group. A molecule of the simple oxalic acid consists of only two carboxylic groups. Oxalic acid salts are frequently present in kidney stones. [Pg.96]

Functionalization Chemical action consisting in functionalizing (adding functional chemical groups) a molecule or the surface of a solid, by chemical synthesis or grafting... [Pg.900]

Step 2 Protonation of the carboxylic acid increases the positive character of its carbonyl group. A molecule of the alcohol acts as a nucleophile and bonds to the carbonyl carbon. [Pg.755]

Group A Molecules. These molecules have spherically symmetric electron shells. Examples are noble gases and the saturated hydrocarbons, which have only sigma bonds between the carbon atoms. Molecules of this type interact nonspecifically, through dispersive forces resulting from concordant electronic motion in the interacting molecules. [Pg.608]

Asymmetric is the term used to describe a C atom with four different substituent groups. A molecule with such a C atom is chiral. [Pg.1366]


See other pages where Group A molecules is mentioned: [Pg.812]    [Pg.812]    [Pg.433]    [Pg.267]    [Pg.106]    [Pg.106]    [Pg.819]    [Pg.102]    [Pg.239]    [Pg.219]    [Pg.294]    [Pg.348]    [Pg.433]    [Pg.468]    [Pg.488]    [Pg.433]    [Pg.252]    [Pg.756]    [Pg.468]    [Pg.756]    [Pg.219]    [Pg.117]    [Pg.796]    [Pg.1253]    [Pg.253]    [Pg.131]    [Pg.608]    [Pg.609]    [Pg.441]    [Pg.394]    [Pg.448]    [Pg.152]   
See also in sourсe #XX -- [ Pg.608 ]




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Attaching a Methyl Group to Various Molecules

Point group of a molecule

Stepwise coupling of groups in a molecule

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