Answer:
Compound A and compound B are constitutional isomers with molecular formula C3H7Cl.
When compound A is treated with sodium methoxide, a substitution reaction predominates. When compound B is treated with sodium methoxide, an elimination reaction predominates.
Explanation:
Constitutional isomers are the one which differs in the structural formula.
When compound A is treated with sodium methoxide, a substitution reaction predominates.
That means sodium methoxide is a strong base and a strong nucleophile.
But when it reacts with primary alkyl halides it forms a substitution product and when it reacts with secondary alkyl halide it forms mostly elimination product.
The reaction and the structures of A and B are shown below:
The balanced equation for the reaction is as follows
2H₂ + O₂ --> 2H₂O
stoichiometry of H₂ to O₂ is 2:1
number of H₂ moles - 30.0 g / 2 g/mol = 15 mol
number of O₂ moles - 80.0 g / 32 g/mol = 2.5 mol
limiting reactant is the reagent in which only a fraction is used up in the reaction
if H₂ is the limiting reactant
if 2 mol of H₂ requires 1 mol of O₂
then 15 mol of H₂ requires 1/2 x 15.0 = 7.5 mol of O₂
but only 2.5 mol of O₂ is required
this means that O₂ is the limiting reagentt and H₂ is in excess
<span>Here we are asked to know the type of bond
between a glycosidic bond. A glycosidic bond is a type of bond that
exists between a carbohydrate molecule to another carbohydrate molecule. A
glycosidic bond creates between two monosaccharides can also be called as an
ether bond.</span>
Answer: Use Avogadro's number, NA = 6.02 × 1023 atoms/mol.
Explanation:
The answer is A: Between 50 and 5,000 amino acids
