By Enid Blyton
It's their first actual event and the key Seven super-sleuths are already at the path of a secret! the group are wearing cover, following a result in a spooky previous condo within the snow...
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Whereas using the Black within the Everglades sooner or later, Alec meets a guy astride a ghostly grey mare. Alec's fascination with the fellow turns to worry as he realizes the guy is dangerously with reference to madness. quickly Alec and the Black are stuck up in a dangerous chase throughout the depths of the Everglades, the place a misstep can be deadly.
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Extra resources for The Secret Seven (Secret Seven, Book 1)
C h e m i c a l Properties In the following Sections the chemical properties of biguanide and its derivatives are systematically considered. Attention may be drawn to the particularly extensive and detailed recent studies concerning biguanides 412 The Chemistry of Biguanides as sources of guanamines and pyrimidines (Section H). The basic nature and properties of biguanides have already been dealt with in Section VI B. A. Thermal Decomposition 1. Arylbiguanides The thermal decomposition of phenylbiguanide, both in the presence and absence of ammonium chloride and aniline hydrochloride, has been studied in some detail (669) with the following results (equations 1 and 2, R ----Ph) : R _ N H .
The reaction has been extended to 1,1disubstituted biguanides (548) and to several other examples (767, 527). 419 F. Kurzer and E. D. Pitchfork H . Condensation w i t h Esters The reaction of biguanides with esters was first studied in detail by Rackmann (578) who showed that ethyl formate and arylbiguanides gave 2,4-diamino-6-substituted s-triazines (LXXXIII, where R', R" and R" may vary widely). ~NIII q- AlkOH +HgO NHR' (LXXXm} 1. Saturated Esters In 1940, phenylbiguanide and ethyl formate were reported (735) to react at room temperature to give a triazine, also formed on fusion of phenylbiguanide and diphenylformamide at 145 ~ Further experience gained with Paludfine (t55)showed that the products were N~-arylguanamines (LXXXII[; R ' = P h , R ' : R m = H ; or R'=p-C1C~H4; R*=Pr~; R " ~ H).
In the presence of too high a concentration of acid, however, amidinoureas will result (572, 730). Thus, the appropriate reactants give the desired 1-arylbiguanides in boiling 12% hydrochloric acid, but yield N-amidino-N'arylureas in 22% acid. Since 22% hydrochloric acid converts the biguanide into the amidinourea (730), support is provided for the primary formation of the biguanides. NH2 II n 0 NFI A r N H 2 + HsN" C. N H . CN 22% HCI Zl NH ""~0/-"* A r N H 9C- N H . C. N H s II Ii NH NH Time, as well as acid concentration, is a factor controlling the nature of the product.
The Secret Seven (Secret Seven, Book 1) by Enid Blyton