Handbook of the polariscope and its pracitcal applications / adapted from the German editon of H. Landolt, by D.C. Robb and V.H. Veley.

  • Hans Heinrich Landolt
Date:
1882
Catalogue details

Licence: Public Domain Mark

Credit: Handbook of the polariscope and its pracitcal applications / adapted from the German editon of H. Landolt, by D.C. Robb and V.H. Veley. Source: Wellcome Collection.

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    a. Ethylidene- lactic Acid C3 Group. Active. (C H3)-*C H (0 H)—(C 0.0 H). Inactive. b. Ethylene-lactic Acid Propionic Acid Glycerine Tartronic Acid Malonic Acid (CH2.0 H) - CH2 - (C 0.0 H). (CH3)-CH2-(CO.OH). (C H2.0 H) - C H (0 H) - (C H2.0 H). (CO. OH) -CH(OH) - (CO. OH). (C 0 . OH) -CH2 — (C0.0 H). c. Propylene-glycol G-lyceric Acid a-Bromo-propionic Acid 0-Dibromo-propionic Acid Propylene - dichloride Propylene - chlorhydrin (C H3) - *c H (0 H) - (C H2.0 H). (C H2.0 H) — *c H (O H) - (CO.OH). (CH3) — *CHBr — (CO. OH). (C H2 Br) — *CHBr — (C 0.0 H). (c H3) — *C H Cl — (C H, Cl). (CH3)-*CH(0H)-(CH,C1). C4 Group. Active. a. Tartaric Acid Tartramide Malic Acid Malamide Asparagin Aspartic Acid (C 0.0 H) - *CH (OH) - [*CH (OH) - (CO.OH)]. (C O . N H2) — *CH (OH) — [*CH (OH) — (C0.NH2)1. (CO.OH — C H2) — *CH(0 H) — (CO.OH). (CO.NH2 — CH2) — *C H (0 H) — (CO.NH2). (CO.NH2-CH2)-*CH(NH,) — (CO.OH). (CO.OH — C H2) — *CH(N H2) — (CO.OH). Inactive. y Succinic Acid Normal Butyric Acid Iso-butyric Acid Butyramide Eumaric Acid (CO.OH) (CH3-CH2) (ch3) (CH3-CH2) (CO.OH) Erythrite (C H2.0 H) Monobromo-succinic Acid (CO.OH) Dibromo- succinic Acid (CO.OH) Dimethyl-succinic Acid (CO.OH) Pyro-tartaric Acid (CO.OH) Secondary Butyl-alcohol (CH3) 0-Butylene Glycol (CH3) a-Hydroxy-butyric Acid (C H3 — C H2) 0-Ditto ditto (CH,)' Aidol (CH3). Chlorobutyl - aldehyde (C H3 — C H2) - Normal Butylene Dibromide (CH3-CH2) - -CH2 — (CH, — CO.OH). -CH2 — (CO.OH). -CH(CH3) — (CO.OH). -CH, — (CO.NH2). - CH = (CH — C 6. OH). - *CH (OH)—[*CH (OH) - (CH,. OH)]. - *C H Br — (CHj — CO.OH). -*CHBr — [*C H Br — (CO.OH)]. - *CH (CH3) - [*CH (CH3)—(CO. OH)]. - *CH(CH3) — (CH2 — CO . OH). - *C H (O H) — (C H2 — C H3). -*CH(0H) - (CH0 — CH2.0H). - *CH(OH) — (CO.OH). -*CH(OH) — (C H, — CO.OH). ■*CH(OH) — (C H, — C HO). *CHC1 — (CHO). • *C H Br — (C H2 Br).