
Interpretation:
The statement '' water not used to extinguish most fires in an organic laboratory" should be explained. Also, the safety issues with the given scenario should be explained.
Concept introduction:
The interaction of water and organic compounds makes them unusable as a fire control measure in an organic laboratory. Organic compounds are generally lighter than water and thus float on water. When water is used as a control measure to put out fire the fire is spread due to the flow of water.
An organic laboratory is guided to follow a set of precautious measures which helps in reducing the risks of accident breakout. These measures include use proper disposal and aeration of labs.

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Chapter 2 Solutions
Owlv2 With Labskills, 4 Terms (24 Months) Printed Access Card For Williamson/masters' Macroscale And Microscale Organic Experiments, 7th
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- Synthesize N-Methylcyclohexylamine from cyclohexanol using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forwardIf possible, please provide the formula of the compound 3,3-dimethylbut-2-enal.arrow_forwardSynthesize 1,4-dibromobenzene from acetanilide (N-phenylacetamide) using the necessary organic or inorganic reagents. Draw the structures of the compounds.arrow_forward
- Indicate the products obtained by mixing (3-oxo-3-phenylpropyl)triphenylphosphonium bromide with sodium hydride.arrow_forwardWe mix N-ethyl-2-hexanamine with excess methyl iodide and followed by heating with aqueous Ag2O. Indicate the major products obtained.arrow_forwardIndicate the products obtained by mixing acetophenone with iodine and NaOH.arrow_forward
- Indicate the products obtained by mixing 2-Propanone and ethyllithium and performing a subsequent acid hydrolysis.arrow_forwardIndicate the products obtained if (E)-2-butenal and 3-oxo-butanenitrile are mixed with sodium ethoxide in ethanol.arrow_forwardQuestion 3 (4 points), Draw a full arrow-pushing mechanism for the following reaction Please draw all structures clearly. Note that this intramolecular cyclization is analogous to the mechanism for halohydrin formation. COH Br + HBr Brarrow_forward
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