Answer:
See the image 1
Explanation:
If you look carefully at the progress of the SN2 reaction, you will realize something very important about the outcome. The nucleophile, being an electron-rich species, must attack the electrophilic carbon from the back side relative to the location of the leaving group. Approach from the front side simply doesn't work: the leaving group - which is also an electron-rich group - blocks the way. (see image 2)
The result of this backside attack is that the stereochemical configuration at the central carbon inverts as the reaction proceeds. In a sense, the molecule is turned inside out. At the transition state, the electrophilic carbon and the three 'R' substituents all lie on the same plane. (see image 3)
What this means is that SN2 reactions whether enzyme catalyzed or not, are inherently stereoselective: when the substitution takes place at a stereocenter, we can confidently predict the stereochemical configuration of the product.
Is there an image with this question
The lower you go, the more acidic. The higher you go, the more alkaline. Your answer would most likely be 6.
P x V = n x R x T
P x 73 = 2.97 x 0.082 x 298
P x 73 = 72.57492
P = 72.57492 / 73
P = 1.0 atm
hope this helps!
Answer: The reaction is exothermic reaction as the energy of products is less than the energy of reactants.
Explanation: Exothermic reactions are defined as the reactions in which energy of the product is less than the energy of the reactants. The total energy is released in the form of heat and 
for the reaction comes out to be negative.
Labeling of the parts in the diagram:
A represents the activation energy which is the energy required by reactants to cross the energy barrier to get converted to products.
E represents the potential energy of the reactants.
B represents the activated complex.
D represents the potential energy of the products.
C represents the total enthalpy change of the reaction, which comes out to be negative for exothermic reactions.
