1answer.
Ask question
Login Signup
Ask question
All categories
  • English
  • Mathematics
  • Social Studies
  • Business
  • History
  • Health
  • Geography
  • Biology
  • Physics
  • Chemistry
  • Computers and Technology
  • Arts
  • World Languages
  • Spanish
  • French
  • German
  • Advanced Placement (AP)
  • SAT
  • Medicine
  • Law
  • Engineering
vova2212 [387]
3 years ago
13

When an unknown amine reacts with an unknown acid chloride, an amide with a molecular mass of 163 g/mol (M = 163 m/z) is formed.

In the infrared spectrum, important absorptions appear at 1661, 750 and 690 cm–1. The 13C NMR and DEPT spectra are provided below. Draw the structure of the product as the resonance contributor lacking any formal charges.

Chemistry
1 answer:
DanielleElmas [232]3 years ago
6 0

Answer:

            As the molecular mass of given amine is 163 g/mol (a odd number) it means that this compound contains a odd number of Nitrogen atoms. We will first apply Rule of Thirteen to get the molecular formula.

Rule of Thirteen:

First divide the parent peak value by 13 as,

                = 163 ÷ 13

                = 12.53

Now, multiply 13 by 12,

                = 13 × 12 (here, 12 specifies number of carbon atoms)

                = 156

Now subtract 156 from 163,

                = 163 - 156

                = 7

Add 7 into 12,

                = 7 + 12

                = 19 (hydrogen atoms)

So, the rough formula we have is,

                                                       C₁₂H₁₉

Now, add one Nitrogen atom to above formula and subtract one Carbon and 2 Hydrogen atoms as these numbers are equal to atomic mass of Nitrogen atom as,

                C₁₂H₁₉   -------N-------->    C₁₁H₁₇N

Also, as shown in ¹³C-NMR there is one peak around 180 ppm and the peak at 1661 cm⁻¹ in IR spectrum is characteristic to carbonyl group hence, we will add one oxygen atom to the chemical formula accordingly. i.e.

                C₁₁H₁₇N   -------O-------->    C₁₀H₁₃NO

Molecular Formula: C₁₀H₁₃NO

Also,

In NMR the the four peaks around 120 ppm are assigned to a mono substituted benzene ring.

The absence of IR peak above 3200 cm⁻³ also confirms that the amine is tertiary in nature and there is no hydrogen attached to the nitrogen atom.

It can be observed that the peaks in upfield are duplicating. This can be due to the presence of rotamers of said compound.

The most plausible structure for given data is shown below, and the resonance structure along with rotamers are also shown.

You might be interested in
Pls help! 2CO + O2 → 2CO2
jok3333 [9.3K]

The bond energy of each carbon-oxygen bond in carbon dioxide is d. 736 kJ

Since the chemical reaction is 2CO + O₂ → 2CO₂ and the total bond energy of the products carbon dioxide CO₂ is 1,472 kJ.

Since from the chemical reaction, we have 2 moles of CO₂ which gives 1,472 kJ and there are two carbon-oxygen, C-O bonds in CO₂, then

2 × C-O bond = 1,472 kJ

1 C-O bond = 1.472 kJ/2

C-O bond = 736 kJ

So, the bond energy of each carbon-oxygen bond in carbon dioxide is d. 736 kJ

Learn more about bond energy here:

brainly.com/question/21670527

7 0
3 years ago
Read 2 more answers
Many scientist compare the parts of a cell to the parts of a factory. Do you think this comparison is fair and useful?
Fittoniya [83]
Yes. Parts of a cell work together just like stations in a factory.
4 0
3 years ago
If a reaction is reversible what are the relative amounts of reactant and product
Alina [70]
<span>If a reaction is reversible, then it will attain the phase of Equilibrium and at that phase, the Amount of Reactants and Products would be:  Equal

Hope this helps!</span>
3 0
3 years ago
Read 2 more answers
Complete the mechanism for the base-catalyzed opening of the epoxide below by adding any missing atoms, bonds, charges, nonbondi
worty [1.4K]

Complete Question:

check the first image for complete part of the question

Answer and Explanation:

Epoxide is a three membered ring made up of two carbon atoms and one oxygen atom. Epoxides are cyclic ethers. Due to its ring size, it is highly strained and very reactive. Epoxide ring opening takes place with respect to addition of acid and base.

Ring opening of epoxide with acid:  

In the presence of base, the nucleophile attacks the epoxide ring at more substituted site and inverse stereochemistry takes place.(check file 2 attached)

Ring opening of epoxide with base:  

The backside attack of nucleophile takes place in less substituted site and then it undergoes protonation to form a product.

(check file 2 attached)

3 0
3 years ago
How many electrons are in the 3p sublevel of Sulfur?
goldenfox [79]
There are FOUR electrons in the 3p sub-level of sulfur....
3 0
3 years ago
Other questions:
  • Iron is impermeable to air and water true or false
    5·1 answer
  • Which conditions are likely to follow the current conditions in the area? Select three responses.
    6·2 answers
  • In which block of the periodic table is chromium (Cr) found? s block d block p block f block
    7·2 answers
  • 9. The broken appearance of pencil in a glass of water is due
    8·1 answer
  • A forest ecosystem starts with both Sonoran toads and Wood frogs. What would you expect to happen if the ecosystem becomes more
    15·1 answer
  • Please help
    7·1 answer
  • How do you account for the formation of ethane during chlorination of methane​
    8·2 answers
  • Would you expect manganese(II) oxide, MnO, to react more readily with HF(aq) or NaOH(aq)?
    5·1 answer
  • How does burning fossil fuels cause an increase of carbon in the air?
    6·2 answers
  • As the temperature of a gas increases, _____. (select all the options that correctly complete the sentence.)
    13·1 answer
Add answer
Login
Not registered? Fast signup
Signup
Login Signup
Ask question!