Your answer to that question is Fand N
Answer:
<em>C. The electron-withdrawing fluorine atoms pull electron density from the oxygen in trifluoroacetate. The negative charge is more stabilized in trifluoroacetate by this effect.</em>
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Explanation:
<em>The structures of trifluoroacetate and acetic acid are both shown in the image attached.</em>
<em>The trifluoroacetate anion (CF3CO2-), just like the acetate anion has in the middle, two oxygen atoms.</em>
<em>However, in the trifluoroacetate anion, there are also three electronegative fluorine atoms attached to the nearby carbon atom attached to the carbonyl, and these pull some electron density through the sigma bonding network away from the oxygen atoms, thereby spreading out the negative charge further. This effect, called the "inductive effect" stabilizes the anion formed,the trifouoroacetate anion is thus more stabilized than the acetate anion.</em>
<em>Hence, trifluoroacetic acid is a stronger acid than acetic acid, having a pKa of -0.18.</em>
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<u><em>Hope this helps!</em></u>
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Answer:
Because Scientists Uses hypothesis and try tests and try proving their points while regular normal people use it to just state a statement
Answer:
An example of engineering material, <em><u>are plastics,</u></em> they are derived from organic, natural materials, such as cellulose, coal, natural gas, salt and, of course, oil. Oil is a complex mixture of thousands of compounds and must be processed before being used.
Explanation:
Plastic production begins with distillation at a refinery, where crude oil is separated into groups of lighter components, called fractions. Each fraction is a mixture of hydrocarbon chains (chemical compounds formed by carbon and hydrogen) that differ in terms of the size and structure of their molecules. One of those fractions, naphtha, is the essential compound for the production of plastic.
Two main processes are used to make plastic: polymerization and polycondensation, and both require specific catalysts. In a polymerization reactor, monomers like ethylene and propylene join to form long polymer chains. Each polymer has its own properties, structure and dimensions depending on the type of basic monomer that has been used.
Answer:
are easily broken
Explanation:
The double covalent bond within unsaturated hydrocarbons are easily broken.
