Enanthotoxin is an extremely poisonous organic compound found in hemlock water drop- wart, which is reputed to be the most poisonous plant in England. It is believed that no British plant has been responsible for more fatal accidents. The most poisonous part of the plant is the roots, which resemble small white carrots, giving the plant the name"five finger death."Also poisonous are its leaves, which look like parsley. Enanthotoxin is thought to interfere with the Nat current in nerve cells, which leads to convulsions and death. он How many stereoisomers are possible for enanthotoxin?

First, draw your chosen compounds including any non-bonding electrons and non-zero formal charges Circle and name any pH-sensitive functional groups. Choose an organic solvent that will dissolve both or your compounds and an aqueous solution (i.e. conc. aqueous NaOH, 5% aq. NaHCO3, or 3M HCl) that would successfully separate the two compounds selected.

In an attempt to synthesize compound C through a two-step process, a chemist discovered after completing the first step that they had inadvertently produced two distinct compounds, A and B. Upon examining the infrared spectroscopy (IR) results, it was observed that both A and B exhibited peaks indicative of a ketone and an ester group. Please provide the molecular structures of A and B. OEt NaOEt ΕΙΟ A B In a chemical experiment, they noticed that both components, A and B, from a combined sample turned into a new compound, C, during the following stage. The task is to determine what compound C looks like and explain how compound A or B changes into compound C through a reaction. Compound C should be the primary molecule containing carbon created in this process, not just a by-product. A B H3O+, H₂O, A Mechanism = с

What is  the pharmacological and pharmacokinetic properties of Phenobarbital? Don't forget to give references

Look at the structures of aniline, N-methyl aniline and Triethylamine rank these compounds in order of increasing solubility in water.

Please explain Frost Circles for aromatic systems and how they can be used to explain the stability of aromatic systems and the instability of anti-aromatic systems.

Which pesticide doesn't have a halogen functional group?ImazapyrNitisinone2,4,5-Trichlorophenoxyacetic acidSimazineAll of these have a halogen

In the mid-1930s a substance was isolated from a fungus that is a parasite of ryes and other grasses. This alkaloid, lysergic acid, has been of great interest to chemists because of its strange, dramatic action on the human mind. Many derivatives of lysergic acid are known, some with medicinal applications. Perhaps the best known derivative of lysergic acid is the potent hallucinogen lysergic acid diethylamide (LSD): మగవా జి N-H LSD (CH25N;O) Like other alkaloids, LSD is a weak base, with Kp = 7.6 × 107. What is the pH of a 0.94 M solution of LSD? pH =

is this correct? Paracetamol consists of an aromatic ring to which a hydroxy group (-OH) is attached, forming a phenol. Attached to the aromatic ring is also an acetamide group, which consists of an acetyl group bound to a nitrogen atom.

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