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Sloan [31]
3 years ago
10

Identify the Lewis acid and Lewis base in each reaction:

Chemistry
2 answers:
nikdorinn [45]3 years ago
8 0

Answer:

The answers to the question are

(a)

  • Fe₃⁺ = Lewis acid
  • H₂O = Lewis base

(b)

  • H₂O = Lewis acid
  • H⁻ = Lewis base

(c)

  • CO⁺ = Lewis acid
  • Ni = Lewis base

Explanation:

Lewis theory of acids states that

An acid is a substance that accepts a pair of electrons an i doing so forms a covalent bond with the group that supplies the electrons

A Lewis base is a substance that donates an unshared pair of electrons to a recipient species with which the  electrons can be shared

(a) Here Fe₃⁺ is the Lewis acid as it accepts an electron pair from H₂O which is amphoteric an so can act either as a Lewis base or acid

Fe₃⁺ = Lewis acid

H₂O = Lewis base

(b) H₂O + H⁻ → H₂ + OH⁻

Here the water accepts a pair of electrons from H⁻ anion hence it is the Lewis acid while H⁻ anion donates a pair of electrons acting as the Lewis base

H₂O = Lewis acid

H⁻ = Lewis base

(c) 4CO⁺ +Ni ↔ Ni(CO₄) Here we have

CO⁺ = Lewis acid

Ni = Lewis base

dybincka [34]3 years ago
5 0

Answer:

Explanation:

A Lewis acid is defined as a chemical species that contains an empty orbital which accepts an electron pair from a Lewis base to.

A Lewis base is defined as any species that has a filled orbital containing an electron pair which is not involved in bonding but forms a dative bond with a Lewis acid.

A. Fe3+ + 2H2O --> FeOH2+ + H30+

Fe3+ - Lewis acid

H2O - Lewis base

B. H2O + H- --> H2 + OH-

H- - Lewis acid

H2O - Lewis base

C. 4CO + Ni --> Ni(CO)4

CO - Lewis base

Ni - Lewis acid

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attashe74 [19]

Answer:

2.29 g of N2

Explanation:

We have to start with the <u>chemical reaction</u>:

NaN_3~->~Na~+~N_2

The next step is to <u>balance the reaction</u>:

2NaN_3~->~2Na~+~3N_2

We can continue with the <u>mol calculation</u> using the molar mass of

NaN_3 (65 g/mol), so:

3.55~g~NaN_3\frac{1~mol~NaN_3}{65~g~NaN_3}=0.054~mol~NaN_3

Now, with the<u> molar ratio</u> between NaN_3  and N_2  we can <u>calculate the moles</u> of N_2  (2:3), so:

0.054~mol~NaN_3\frac{3~mol~N_2}{2~mol~NaN_3}=0.0819~mol~N_2

With the molar mass of N_2 we can <u>calculate the grams</u>:

0.0819~mol~N_2=\frac{1~mol~N_2}{28~g~N_2}=2.29~g~N_2

I hope it helps!

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An object that is traveling around another body in space is in ______ around that body
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An object that is traveling around another body in space is in ORBIT around that body
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Determine the primary structure of an octapeptide from the following data: acid-catalyzed hydrolysis gives 2 arg, leu, lys, met,
erma4kov [3.2K]

Complete Question

The complete question is shown on the first uploaded image

Answer:

The sequence of these amino acid would be

          <u>Lue</u>  <u>Arg</u>  <u>Lys</u>  <u>Arg</u>  <u>Met</u>  <u>Phe</u> <u>Arg</u>  <u>Ser</u>

Explanation:

The acid-catalyzed hydrolysis from makes us to understand that the  polypeptides contains 8 amino acids

   From the question we are told that the Edman's reagent releases Leu it means that the N-terminal amino acid would be Lue(i.e Leucine)

     Also from the question we are told that the Carboxypeptidase  released Ser this mean the the C-terminal  amino acid would be Ser ( i.e Serine)

   The Amino acids would in the polypeptides would be arranged like this  

         

         <u>Lue</u> __  __  __  __  __ __  <u>Ser</u>

Now from the question we are told that treatment with cranogen bromide form two peptides.

   Now generally  cranogen bromide divides a peptide on  the C- side(i.e the extreme left side ) of  Met(Methionine)(This is an amino acid obtained by hydrolysis of most common peptides )

   So this means that any peptides  containing Met(Methionine) must have Methionine as a C- terminal amino acid(i.e at extreme left) and for peptides that does not contain Met must be C - terminal peptides

From the question we see that it is the second peptide that contain Met and it is a penta peptide(i.e it contains 5 amino acid)  

    Thus the fifth amino acid is  Met  

So the sequence of these amino acid would now be  

          <u>Lue</u> __  __  __  <u>Met</u>  __ __  <u>Ser</u>

From the question we are told that the the Trypsin-catalyzed hydrolysis forms two amino acid and two peptides  

   Now generally Trypsin divides a peptide  on the  C- side(i.e the extreme left) of Arg(Arginine) and Lys (lysine) and any peptide that holds Arg or Lys  must have them as their C- terminal  amino acids

   From the first peptide in the two peptide formed we see that  Arg would be the Seventh amino acid of the octapeptide because commonly the trypsin that sticks to the C-side of Arg would for Ser

and Phe would be the sixth amino acid of the octapeptide

So the sequence of these amino acid would be

       <u>Lue</u> __  __  __  <u>Met</u>  <u>Phe</u> <u>Arg</u>  <u>Ser</u>

Looking  at the first amino acid formed from the Trypsin-catalyzed hydrolysis  we see that Arg would be the fourth amino acid of  octapeptide      as Trypsin divides a peptide  on the  C- side(i.e the extreme left) of Arg(Arginine).

From the second peptide of the  Trypsin-catalyzed hydrolysis  we see that Lys would be the third amino acid of the octapeptide as trypsin divides on the  C- side of  Lys (lysine) and Tyr would be the second amino acid of the octapeptide

So the sequence of these amino acid would be

          <u>Lue</u>  <u>Arg</u>  <u>Lys</u>  <u>Arg</u>  <u>Met</u>  <u>Phe</u> <u>Arg</u>  <u>Ser</u>

           

4 0
3 years ago
Use the following structures of amino acids to answer the questions below. Note that the difference in the structures (the side
alexira [117]
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