Answer:
88.50 %
The balance chemical equation is as follow,
2 H₂ + O₂ → 2 H₂O
Step 1: Find the limiting reactant;
According to eq.
4.032 g (2 mole) H₂ reacts with = 32 g (1 mole) of O₂
So,
11 g of H₂ will react with = X g of O₂
Solving for X,
X = (11 g × 32 g) ÷ 4.032 g
X = 87.301 g of O₂
Therefore, H₂ is the limiting reactant as O₂ is present in excess.
Step 2: Calculating %age Yield;
According to eq.
4.032 g (2 mole) H₂ produces = 36.032 g (1 mole) of H₂O
So,
11 g of H₂ will react with = X g of H₂O
Solving for X,
X = (11 g × 36.032 g) ÷ 4.032 g
X = 98.301 g of H₂O
So,
Actual Yield = 87 g
Theoretical Yield = 98.301 g
Using formula = Actual Yield / Theoretical Yield × 100
= 87 g / 98.301 × 100
= 88.50 %
Answer:
a) Attached below
b) The presence of racemic mixture found as product in both cases shows that products are identical ( i.e. they have same configuration
Explanation:
Diagrams of the products obtained from hydroboration-oxidation of cis-2-butene , hydroboration-oxidation of trans-2-butene.
attached below
The presence of racemic mixture found as product in both cases shows that products are identical ( i.e. they have same configuration )
Answer:
-) Acid-base reaction
-) Carboxylic acid, alcohol, alkene and ketone
Explanation:
For the reaction between acetic acid and triethylamine, we will have an <u>acid-base reaction</u>. Therefore a s<u>alt would be produced</u> in this case an <u>"ammonium quaternary salt"</u>. Also, we have to remember that on this reaction the acid is the acetic acid and the base is the triethylamine. See figure 1
For the second question, we have to check the <u>structure of Prostaglandin</u> E1 in which we have the functional groups:
<u>1) Carboxylic acid</u>
<u>2) Alcohol</u>
<u>3) Alkene</u>
<u>4) Ketone</u>
See figure 2.
I hope it helps!
Answer:
The first step of this ozonolysis produces an acid anhydrous with on hydrolysis gives the same Carboxylic acid
Explanation:
Please find attached the reaction steps