Correct answer is <span>X = ΔH
Reason:
1) The graph of enthalpy Vs reaction coordinate suggest the reaction is endothermic in nature. For endothermic reaction, energy if product is more than that of reactant. Hence, option 1 i.e. </span><span>X = -ΔH cannot be correct.
2) Since the reaction is endothermic in nature, </span>energy if product is more than that of reactant. Hence, option 2 i.e. X = ΔH is correct.
3) Activation energy is energy difference between Reactant (A) and transition state (B). However, as per option C, activation energy (A.E.) is energy difference between product (C) and transition state (B), which is incorrect.
<h2>
Answer: 125.41 mL</h2>
Explanation:
Volume = mass ÷ density
= 116 g ÷ 0.925 g/mL
= 125.41 mL
<h3>A 116 g of sunflower oil of 0.925 g/mL has a volume of 125.41 mL.</h3>
Answer:
The answer is attached below
Explanation:
To draw the Lewis structure the sulphur willl be placed in the centre with the Valence electron sorrounding it the electrons between sulphu and oxygen to form bonds
Answer:
Explanation:
There are few simple rules in organic chemistry which a person must learn.
1. In predicting a structure from ozonolysis, number of oxygen present in products must be counted. In this particular example, there are 2+3+1 = 6 oxygen atoms are present in three molecules. This means that there should be at least three confirmed double bonds must be present in the molecule of Dictyopterene.
2. There are in total of 3+5+3 = 11 carbon atoms present, making 2^11 = 2048 possible structures for this particular structure. But since there are three double bonds present, this will reduce the number of possible structures as well.
3. Questions also says that when fully hydrogenated, the molecule generates Butylcycloheptane. That means that our base molecule is Butylcycloheptane and this molecule contains at least three double bonds.
So, first we draw the molecule of butylcycloheptane. After this, we think of were double bonds could be present. We do have the products. Let's make their structures first. I have also mentioned the possible breakup where the ozonolysis has occured by color code. You can see them in the reference image attached.
Part 1 out of 2: There is only one chiral carbon present in the molecule and have two possible isomers. Cis and Trans. Only one stereogenic carbon is present, that's why two possible isomers. Image attached.