Answer: The actual yield of 
is 60.0 g
Explanation:-
The balanced chemical reaction :
Mass of 
=
According to stoichiometry:
1 mole of gives = 1 mole of
1.51 moles of gives =
moles of
Theoretical yield of 
Percent yield of = 
Thus the actual yield of is 60.0 g
Answer is: D. It is not sodium bicarbonate.
Balanced chemical reaction of heating sodium bicarbonate: 2NaHCO₃ → Na₂CO₃ + CO₂ + H₂O.
This is chemical change (chemical reaction), because new substances are formed (sodium carbonate, carbon(IV) oxide and water), the atoms are rearranged, so there is no sodium bicarbonate (NaHCO₃) in the test tube.
Answer:
amino group
Explanation:
There are twenty (20) amino acids in nature. Generally, each amino acid is structurally made up of a central carbon atom called alpha carbon attached to a hydrogen, carboxylic acid group (-COOH) and an amine group (-NH2). However, one particular amino acid called PROLINE posseses an exception to this.
Proline, which is the only cyclic amino acid, is also the only amino acid that forms a secondary amine group i.e. loss of hydrogen atoms in its amine group when in a protein structure. This means that when in a protein, PROLINE does not have an AMINE GROUP.
Answer:
The answer is "Option b and Option c".
Explanation:
This buffer is a buffer of ammonia and ammonium ion. Thus it requires the solution 
.
In point 1:
The solution containing at 1M concentration would be given by mixing the two solutions. Thus, this buffer is a legitimate route.
In point 2:
It gives the ions you want but they are not the same.
In point 3:
and 
volume would not produce the same concentrations. Therefore, this buffer isn't a valid route.
In point 4:
Some volume and half . This offers the same rate as half.
Explanation:
The - 3 degree C( carbon atom) 2p atomic orbital + methyl C-H sigma molecular orbital because one C-H bond has to dissolve its bond and provide the H that is sigma molecular orbital and the carbonation is type 3 degree sp2 carbon.
Hyperconjugation is the stabilizing effect arising from the electrons ' engagement in a π-bond (usually C-H or C-C) with a neighboring empty or partly filled p-orbital or π-orbital to provide an expanded molecular orbital that enhances system stability.
