Answer: 0.0220275 M
Explanation:
So, we are given the following data or parameters which are going to help in solving this particular Question/problem.
=> Averagely, we have the volume = 5.0 L of blood in human body .
=> Mass of sugar eaten = 37.7 g of sugar (sucrose, 342.30 g/mol).
Therefore, the molarity of the blood sugar change can be calculated as below:
The molarity of the blood sugar change = (1/ volume) × mass/molar mass.
Thus, the molarity of the blood sugar change = (1/5) × 37.7/342.30 = 0.0220275 M.
Answer:
8 moles of C
Explanation:
From the question given above, the following equation was obtained:
3A + 2B —> 6C
From the equation above,
3 moles of A reacted to produce 6 moles of C.
Thus, the number of mole of C produced by reacting 4 moles of A can be obtained as follow:
From the equation above,
3 moles of A reacted to produce 6 moles of C.
Therefore, 4 moles of C will react to produce = (4 × 6)/3 = 8 moles of C
Thus, 8 moles of C can be obtained from the reaction of 4 moles of A with excess B
We are given –
- Final velocity of car is, v= 0
- Initial velocity of car is, u= 100 km/hr
- Time taken, t is = 3 minutes or 180 sec
Here–






Now –
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I think it would be C.100.5cm or D.100.5ml hope that helps
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.