You are going to fall, face first on the ground.
Answer:
The answer to your question is HCl + NaOH ⇒ NaCl + H₂O
Explanation:
Data
Double displacement reaction
Balanced chemical reaction
HCl + NaOH ⇒ NaCl + H₂O
Reactants Elements Products
1 Chlorine (Cl) 1
1 Sodium (Na) 1
2 Hydrogen (H) 2
1 Oxygen (0) 1
As we can see, the reaction is balanced and the coefficients of all reactants and products are 1, but the number is not written in a balanced reaction.
Answer: A)There is a high ratio of energy to cost
Positives:
A Chunk of Uranium can power a city a lot longer than a chunk of coal.
It also does not contribute to pollution since what comes out of the tower is steam.
Negatives:
It is very expensive to build and maintain a nuclear power plant at first so investors whom want money up front are more reluctant to loan money for one.
If the plant does melt down it is very bad for the enviroment and its people, for example Chernobyl Nuclear Power Plant in the Ukraine will not be able to be lived in for approximently 20,000 years.
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.