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H Bromide

H-Bond Donor (HBD) Inorganic acids Active H chlorides Active H fluorides Active H iodides Active H bromides ... [Pg.1318]

Non-Bonding (NB) Paraffins Nonactive H chlorides Nonactive H fluorides Sulfides Nonactive H iodides Disulfides Nonactive H bromides Thiols... [Pg.1318]

MNN is obtained in 3—5% yield by the nitration of naphthalene and is present at this level in coml MNN. It is best prepd by indirect methods for example, by the removal of an amino group from an appropriately substituted nitro-naphthylamine. The amine is treated with Na nitrite and acid to form the diazonium salt which is replaced with a H atom by redn with EtOH (Ref 7). It may also be prepd by treatment of 6-nitro-l, 2,3,4-tetrahydronaphthalene with Br to form a dibromo compn (probably the 1,4-isomer), followed by removal of two moles of H bromide by distn in the presence of base (Ref 10). 2-Naphthalenediazonium fluoroborate... [Pg.191]

See other pages where H Bromide is mentioned: [Pg.90]    [Pg.667]    [Pg.398]    [Pg.378]    [Pg.115]    [Pg.636]    [Pg.1100]    [Pg.1104]    [Pg.1123]    [Pg.1128]    [Pg.1165]    [Pg.1246]    [Pg.1292]    [Pg.153]   


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