Answer:
30.8 grams of magnesium hydroxide will form from this reaction, and magnesium nitrate is the limiting reagent.
Explanation:
The reaction that takes place is:
- 2NaOH + Mg(NO₃)₂ → 2NaNO₃ + Mg(OH)₂
Now we <u>convert the given masses of reactants to moles</u>, using their respective <em>molar masses</em>:
- 68.3 g NaOH ÷ 40 g/mol = 1.71 mol NaOH
- 78.3 g Mg(NO₃)₂ ÷ 148.3 g/mol = 0.528 mol Mg(NO₃)₂
0.528 moles of Mg(NO₃)₂ would react completely with (0.528 * 2) 1.056 moles of NaOH. There are more than enough NaOH moles, so NaOH is the reagent in excess and <em>Mg(NO₃)₂ is the limiting reagent.</em>
Now we <u>calculate how many Mg(OH)₂ are produced</u>, using the <em>moles of the limiting reagent</em>:
- 0.528 mol Mg(NO₃)₂ *
= 0.528 mol Mg(OH)₂
Finally we convert Mg(OH)₂ moles to grams:
- 0.528 mol Mg(OH)₂ * 58.32 g/mol = 30.8 g
Answer:
Carbohydrates can be divided into two main types: simple and complex. Simple carbohydrates are made up of just one or two sugar units, whereas complex carbohydrates are made up of many sugar units.
Answer:The product formed on reaction with hydroxide ion as nucleophile is 2R-hexane-2-ol.
The product formed on reaction with water would be a 50:50 mixture of
2S-hexane-2-ol. and 2R-hexane-2-ol.
Explanation:
2S-iodohexane on reactiong with hydroxide ion would undergo SN² substitution reaction that is substitution bimolecular. Hydroxide ion has a negative charge and hence it is a quite good nucleophile .
The rate of a SN² reaction depends on both the substrate and nucleophile . Here the substrate is a secondary carbon center having Iodine as a leaving group.SN² reaction takes place here as hydroxide ion is a good nucleophile and it can attack the secondary carbon center from the back side leading to the formation of 2R-hexane-2-ol.
In a SN² reaction since the the nucleophile attacks from the back-side so the product formation takes place with the inversion of configuration.
When the same substrate S-2-iodohexane undergoes a substitution reaction with water as a nucleophile then the reaction occurs through (SN¹) substitution nucleophilic unimolecular mechanism .
The rate of a SN¹ reaction depends only on the nature of substrate and is independent of the nature of nucleophile.
The SN¹ reaction is a 2 step reaction , in the first step leaving group leaves leading to the formation of a carbocation and once the carbocation is formed then any weaker nucleophile or even solvent molecules can attack leading the formation of products.
In this case a secondary carbocation would be generated in the first step and then water will attack this carbocation to form the product in the second step.
The product formed on using water as a nucleophile would be a racemic mixture of R and S isomers of hexane -2-ol in 50:50 ratio. The two products formed would be 2R-hexane-2-ol and 2S-hexane-2-ol.
Kindly refer the attachment for reaction mechanism and structure of products.
