Question:

Polarisation of electrons in acrolein may be written as

Updated On: Jul 4, 2024
  • $^{\delta+}_{CH_2 =CH -}\, ^{ \, \, \, \, \, \, \, \, \, \, \, \delta-}_{CH=O}$
  • $^{\delta+}_{CH_2 =}\, ^{ \delta+}_{CH-CH=O}$
  • $^{\delta+}_{CH_2 =CH -}\, ^{ \, \, \, \, \, \, \, \, \, \, \, \delta+}_{CH=O}$
  • $^{\delta-}_{CH_2 =CH -}\, ^{\delta+}_{CH=O}$
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The Correct Option is A

Approach Solution - 1

In $CH_2 = CH-CHO$ due to - M-effect of -CHO group, polarisation of electron takes place as follows:
Hence, partial polarisation is represented as $\hspace20mm $$^{\, \, \, \delta+}_{CH_2 =CH -}\, ^{\, \, \, \, \, \, \, \, \, \, \, \delta-}_{CH=O}$
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Approach Solution -2

Due to the difference in the electronegativity of any two bonding atoms, a phenomenon known as polarization occurs when a portion of an object acquires a partial positive or partial negative charge.
The propensity of an atom to draw a bonded pair of electrons towards itself is known as electronegativity. If the two atoms have even a minor difference in their electronegativity during the bonding process, the electron will be drawn more strongly to the more electronegative atom, which will cause it to gain a partial negative charge. However, the electron will now take up a partial positive charge since it has been slightly moved to the opposite side of a less electronegative atom.
In this manner, polarization takes place, and we can quickly determine whether an atom in the molecule will be partially positive or negatively charged by examining the electronegativity trend.
Similar to this, there are carbon atoms and an oxygen atom in acrolein. There won't be any partial charge on nearby carbon atoms since the electronegativity of all carbon atoms is the same.
Oxygen will have a partial negative charge, whereas carbon will have a partial positive charge because oxygen is more electronegative than carbon.

 
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Top Questions on Structural Representations Of Organic Compounds

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Concepts Used:

Structure of Organic Compounds

The three structural formulas – complete structure, condensed structure, and bond line structural formulas are explained below:

Complete Structural Formula-

The Lewis dot structure is considered as the complete structural formula. In Lewis structure, the covalent bonds in the compound are denoted by a dash (―). This helps to emphasize the number of bonds formed by the electrons. Every single bond, a double bond, and a triple bond are represented by one dash, double dash, and triple dash respectively. It illustrates every single bond formed between every atom in the compound, thus called complete structural formula.

Condensed Structural Formula-

Since complete structural formula consumes much time and space to represent the structure, we can condense them. This is the condensed structural formula, where replacing some dashes/bonds by a number of identical groups attached to an atom by a subscript.

Bond Line Structural Formula-

A bond lines structural formula is another way of structural representation of organic compounds.  Here, every bond is represented as a line in a zigzag manner. If not specified, every terminal is assumed to be a methyl (-CH3) group.