Answer:
the vapor pressure of this solution would increase if some of the water were allowed to evaporate
Answer:
the sun is supposed to in the middle instead of earth since the planets rotate around the sun. on the side Here are the planets listed in order of their distance from the Sun:
Mercury: ...
Venus: ...
Earth: ...
Mars: ...
Jupiter: ...
Saturn: ...
Uranus:
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2355.2 is how many grams there are
Answer:
Based on compounds given, NO reaction occurs
Explanation
The compounds should exchange ions to generate a driving force that pulls the reaction to completion. => Example ...
The Molecular Equation is ...
NH₄Cl(aq) + AgNO₃(aq) => NH₄NO₃(aq) + AgCl(s)
Silver chloride forms in this reaction as a solid precipitate because of its low solubility and is the 'Driving Force' of the reaction. Driving Force is a more stable compound than any on the reactant side and when formed leaves the reaction system as a solid ppt, liquid weak electrolyte (i.e., weak acid or weak base) or a gas decomposition product of a weak electrolyte.
The Ionic Equation is ...
NH₄⁺(aq) + Cl⁻(aq) + Ag⁺(aq) + NO₃⁻(aq) => NH₄⁺(aq) + NO₃⁻(aq) + AgCl(s)
This shows all ions from reaction plus the Driving Force of the reaction.
The Net Ionic Equation is ...
Ag⁺(aq) + Cl⁻(aq) => AgCl(s)
The Net Ionic Equation shows only those ions undergoing reaction. The NH₄⁺ and NO₃⁻ ions are 'Spectator Ions' and do not react.
Attached is a reference sheet for determining the Driving Force of a Metathesis Double Replacement Reaction. Suggest reviewing acid-base theories and the products of decomposition type reactions.
Answer:
See explanation and images attached
Explanation:
a) In the mechanism for the acid catalysed esterification of propanoic acid using ethanol, we can see that the first step is the protonation of the acid followed by nucleophillic attack of the alcohol. Loss of water and consequent deprotonation regenerates the acid catalyst. We can see the fate of the 18O labelled ethanol in the mechanism shown.
b) In the second mechanism, an unnamed ester is hydrolysed using an acid catalyst. The attack of the acid and subsequent nucleophillic attack of water labelled with 18O leads to the incorporation of this 18O into the product acid as shown in the mechanism attached to this answer.