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Alkyl, amines Names

It is known from electrochemical studies that fullerenes are easily reduced. Up to 6 electrons can be added reversibly [19], and, as mentioned earlier, the excited states are even more easily reduced. A large number of electron donors were investigated including aromatic and alkyl amines [29,43,79,119-140,152,161], ni-troxide radicals [57,117], suspensions of Ti02 [118], polyaromatic compounds, [19,127] organo-silicon compounds, [133,158] phenothiazine, [133] acridine [145,154], (3-carotene [141], tetrathiafulvalenes [146], tetraethoxyethene [147], phthalocyanines [148], porphyrines [151,153], NADH and analogues [150,154, 155], borates [156,159], and naphtoles [23] to name a few representative cases. [Pg.658]

B is an amine with two alkyl substituents. Name these groups and identify alkyl hydrogens as primary, secondary or tertiary. [Pg.104]

Metabolites derived by loss of an alkyl or arylalkyl group from ethers [Eq. (4)], thioethers [Eq. (5)], amines [Eq. (6)], and amides [Eq. (7)] represent common biotransformation pathways (R, R" = H, alkyl or aryl). These processes involve oxidation on carbon adjacent to the heteroatom. The intermediates are generally unstable and readily decompose to the corresponding alcohol, thiol, amine, or amide and an aldehyde. Intermediates formed from amides [Eq. (7)] are more stable and may be detected as excreted metabolites. If a secondary carbon atom is adjacent to the heteroatom, then this portion of the molecule is released as a ketone. The heteroatom may also be located in a cyclic structure (e.g., morpholine, piperazine). Two processes have been adopted for amines, namely, N-dealkylation or deamination, that are essentially the same event. In general, which of the two terms applies depends on the... [Pg.312]

An alkyl group name followed by the name of the class of the compound (alcohol, amine, etc.) yields the common name of the compound. The following examples show how alkyl group names are used to build common names ... [Pg.64]

Give each of the following amines a common name by adding the ending -amine to alkyl group names ... [Pg.222]

Most recently the core cross-linking approach was adopted for the preparation of novel nanoassemblies derived from pH-responsive AB diblock copolymers prepared via RAFT (222). Here the A block was the permanently hydrophilic DMA species with the timably hydrophilic/hydrophobic DMBVA forming the B block. In aqueous media, at high pH, these block copolymers form core-shell structures with the DMA residues forming the corona and the DMVBA chains in the core. Addition of a hydrophobic, difimctional, alkyl halide namely 1,4-bisbromomethylbenzene results in this species being sequestered into the hydrophobic core of the micelles where it reactions with the tertiary amine residues via the Menshutkin reaction to yield the core-cross-linked species. Successful core cross-linking was... [Pg.9216]

A primary amine is a compound containing an NH2 group connected to an alkyl group. lUPAC nomenclature allows two different ways to name primary amines. While either method can be used in most circumstances, the choice most often depends on the complexity of the alkyl group. If the alkyl group is rather simple, then the compound is generally named as an alkyl amine. With this approach, the alkyl substituent is identified followed by the suffix "amine." Below are several examples. [Pg.1092]

Much like primary amines, secondary and tertiary amines can also be named as alkyl amines or as alkanamines. Once again, the complexity of the alkyl groups typically determines which... [Pg.1092]

Next, determine whether to name the compound as an alkyl amine or as an alkanamine. If the alkyl groups are simple, then the compound can be named as an alkyl amine otherwise, it should be named as an alkanamine. In this case, one of the alkyl groups is complex, so the compound will be named as an alkanamine. The complex alkyl group is chosen as the parent, and the other alkyl group is listed as a substituent, using the letter N as a locant. Notice that the parent is numbered starting from the side closer to the amine moiety. [Pg.1093]

A two-step process that achieves Markovnikov addition of an alcohol (H and OR) across an alkene. The product of this process is an ether, alkyl amines (Sect. 23.2) A format for naming amines containing simple alkyl groups. [Pg.1296]

Other heterocyclic systems studied include the phenazines [61], triazoles and imidazoles [89] and aziridenes [88]. In the last named the NH bands are more typical of alkyl amines and absorption is between 3360 and 3340 cm" in the vapour. In the liquid state self-association lowers this to 3250—3240 cm" for alkyl aziridenes. When acyl groups are substituted in the ring two NH bands appear corresponding to two different invertomers. Marked variations in both frequency and intensity have been noted by Barr and Haszeldine [60] in NH groups with fluorine substituents at the a-carbon atom. The NH frequency of Z /s-2-2-2-trifluoro-dimethylamine, for example, is 3460 cm", and the extinction coefficient is about 50 times greater than that of dimethylamine itself. [Pg.282]

Name each of the following molecules twice, first as an alkanamine, then as an alkyl amine. [Pg.935]

Hi Name two types of organic compound that can be reduced by LiAlH to form an alkyl amine. [Pg.413]

Common name N,N-bis(2-hydroxyethyl)(coconut oil alkyl)amine ... [Pg.153]

ManufJDistrib. DeWolf Chem. Somerset Cosmetic Co. Variali Trade Names Noram 2C Trade Names Containing Amieen 2C Dlcoco alkyl amine. See DIcocamlne... [Pg.2072]

Amines are named m two mam ways m the lUPAC system either as alkylamines or as alkanamines When primary amines are named as alkylamines the ending amine IS added to the name of the alkyl group that bears the nitrogen When named as alkan amines the alkyl group is named as an alkane and the e ending replaced by amine... [Pg.914]

Alkylamines are named m two ways One method adds the ending amine to the name of the alkyl group The other applies the principles of sub stitutive nomenclature by replacing the e ending of an alkane name by amine and uses appropriate locants to identify the position of the ammo group Arylammes are named as derivatives of aniline... [Pg.955]


See other pages where Alkyl, amines Names is mentioned: [Pg.46]    [Pg.15]    [Pg.142]    [Pg.900]    [Pg.261]    [Pg.900]    [Pg.27]    [Pg.37]    [Pg.7045]    [Pg.15]    [Pg.1289]    [Pg.1377]    [Pg.4523]    [Pg.288]    [Pg.109]    [Pg.213]    [Pg.298]    [Pg.1130]    [Pg.474]    [Pg.479]    [Pg.480]    [Pg.482]    [Pg.62]    [Pg.918]    [Pg.918]    [Pg.918]    [Pg.940]    [Pg.278]    [Pg.393]    [Pg.63]   
See also in sourсe #XX -- [ Pg.49 ]




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