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Not as of September 2010. There appear to be some possible issues regarding groundwater contamination which have delayed any potential approval from the state.

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How is methyl made?

There is no such thing as a lone 'methyl'. A methyl group is a CH3 extending off an organic compounds main carbon chain. They can be created by the Sn2 reaction on iodomethane, or by the reaction of methyl lithium or MeMgCl with a carbon atom that is substituted with a leaving group


What product will be extract using radish?

radish can be a pesticide. radish can be a pesticide.


What is an unintended consequence of using pesticide of plants?

The rise of pesticide-resistant insects.


A farmer wants to know if a new pesticide will produce better tomatoes than his old pesticide. Which of the following is the best hypothesis to use to address his question?

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How can I make elephant toothpaste using potassium iodide?

To make elephant toothpaste using potassium iodide, mix hydrogen peroxide with dish soap and food coloring in a container. Then, add potassium iodide to the mixture and watch as the foam erupts like toothpaste.


What is the test for hydrogen iodide?

Hydrogen iodide can be tested using silver nitrate solution. When hydrogen iodide is bubbled through silver nitrate solution, a yellow precipitate of silver iodide is formed. This confirms the presence of iodide ions in the sample.


What chemicals make tin iodide?

Tin iodide is typically made using tin and iodine. The most common tin iodide is stannous iodide (SnI2) which is produced by combining tin metal with iodine in proper stoichiometric ratios under controlled conditions.


How do you test for presence of iodide ion?

You can test for the presence of iodide ions using silver nitrate. When silver nitrate is added to a solution containing iodide ions, a yellow precipitate of silver iodide forms. This precipitate confirms the presence of iodide ions in the solution.


What is the chemical equation for the preparation of Lugol's solution using potassium iodide and iodine?

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Why would be the effect of carrying out the sodium iodide in acetone reaction with the alkyl halides using an iodide solution half as concentrated?

Carrying out the sodium iodide in acetone reaction with alkyl halides using an iodide solution half as concentrated would likely result in a slower reaction rate and potentially lower yields of the desired product. This is because a lower concentration of iodide ions would decrease the nucleophilicity, reducing the likelihood of effective collisions between the iodide and the alkyl halide. Additionally, the reaction may favor competing pathways or side reactions due to insufficient iodide concentration to drive the desired substitution reaction efficiently.


How do you get rid of lawn?

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