What is the order in which the H1 NMR singals would appear (from most downfield to most upfield) ? For each NMR signal expected, what is the integration value and multiplicity?

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What is the order in which the H1 NMR singals would appear (from most downfield to most upfield) ?

For each NMR signal expected, what is the integration value and multiplicity?

The image is a screenshot of a ChemDraw Professional interface displaying the molecular structure of acetophenone. The ChemDraw interface includes several elements:

1. **Menu Bar**: At the top, featuring options such as File, Edit, View, Object, Structure, Text, Curves, Colors, Search, Add-ins, Window, and Help.

2. **Toolbar**: Below the menu bar, offering various tools for drawing and editing chemical structures, including text formatting options.

3. **Tools Panel**: On the left side, presenting a variety of drawing tools, such as lines, shapes, and chemical symbols.

4. **Main Workspace**: In the center, where the chemical structure is drawn.

5. **Chemical Structure**: A two-dimensional representation of acetophenone, featuring:
   - A benzene ring, depicted as a hexagon with alternating double bonds.
   - A carbonyl group (C=O) attached to an ethyl group and the benzene ring.

This tool is widely used for designing and visualizing chemical structures in educational and professional settings.
Transcribed Image Text:The image is a screenshot of a ChemDraw Professional interface displaying the molecular structure of acetophenone. The ChemDraw interface includes several elements: 1. **Menu Bar**: At the top, featuring options such as File, Edit, View, Object, Structure, Text, Curves, Colors, Search, Add-ins, Window, and Help. 2. **Toolbar**: Below the menu bar, offering various tools for drawing and editing chemical structures, including text formatting options. 3. **Tools Panel**: On the left side, presenting a variety of drawing tools, such as lines, shapes, and chemical symbols. 4. **Main Workspace**: In the center, where the chemical structure is drawn. 5. **Chemical Structure**: A two-dimensional representation of acetophenone, featuring: - A benzene ring, depicted as a hexagon with alternating double bonds. - A carbonyl group (C=O) attached to an ethyl group and the benzene ring. This tool is widely used for designing and visualizing chemical structures in educational and professional settings.
Expert Solution
Step 1

1Hnmr spectra provides the information of hydrogen environments of the unknown compound.

The factors that affect the chemical shift :

Electronegative atoms:

The nmr active nuclei which is directly connected with more electronegative atoms shows downfield shifts. 

Electron withdrawing groups:

The nmr active nuclei which is connected with electron withdrawing group shows downfield shift.

The effect of electronegative atoms is higher than the electron withdrawing groups on the chemical shift.

Splitting of 1Hnmr signals: The splitting follows (n+1) rule. here, n = no. of adjacent hydrogens.

If,

n=0,

0+1=1, singlet,

n=1,

1+1=2, doublet,

n=2,

2+1=3, triplet,

n=3,

3+1=4,quartet

n=4,

4+1=5, quintet.

The integration indicates the no. of hydrogens of each signal of the target 1hnmr active nuclei

 

 

 

 

 

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