The structure of the alkyl bromides used in a malonic ester synthesis of ethyl 2-methyl-4-pentenoate.
Ethyl 2-methyl-4-pentenoate by Malonic ester synthesis.
The alkylation of diethyl malonate or a related ester of malonic acid at the carbon alpha (immediately next) to both carbonyl groups, followed by conversion to a substituted acetic acid, characterizes the chemical reaction known as the malonic ester synthesis.
As a result, it is evident from the structure of ethyl 2-methyl-4-pentenoate that ethyl and methyl bromides are the alkyl bromides employed.
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Answer:
Oxygen is the limiting reactant.
Explanation:
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In this case, given the reaction:
Hence, given the masses of both ethanol and oxygen, we are able to compute the available moles ethanol by:
Next, we compute the moles of ethanol that react with the 0.640 grams of oxygen considering their 1:3 molar ratio in the chemical reaction:
In such a way, since there are 0.01 available moles of ethanol but just 0.0067 moles are reacting, we evidence ethanol is in excess, therefore the oxygen is the limiting reactant.
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PH indicators detect the presence of H+ and OH-. They do this by reacting with H+ and OH-: they are themselves weak acids and bases. If an indicator is a weak acid and is coloured and its conjugate base has a different colour, deprotonation causes a colour change.
