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Write the IUPAC names of the following compounds:


(a) 1, 1 1-Trichloro-2, 2-diphenylethane.
(b) Phenyl 2-methyl propanoate.
(c) 2, 4-Dinitrobenzenamine.

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Giving justification, categorise the following molecules/ions as nucleophile or electrophile:
HS to the power of minus comma space BF subscript 3 comma space straight C subscript 2 straight H subscript 5 straight O to the power of minus comma space left parenthesis CH subscript 3 right parenthesis subscript 3 space straight N semicolon space space CI to the power of circled dash comma space
space space space space space CH subscript 3 space minus space straight C with plus on top space equals space straight O semicolon space space space straight H subscript 2 straight N with bar on top semicolon comma space NO subscript 2 superscript plus.


Nucleophile:
   
These have a unshared pair of electrons which can be donated and shared with an electrophile.
Electrophiles:  
Positive sites have only six valence electrons, can accept pair from a nucleophile.

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Give the IUPAC names of the following:



2 - Chlorocyclohoexanol             4 - Nitrocyclohexanal

(iii)
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Using the curved-arrow notation, show the formation of reactive intermediate when the following covalent bonds undergo heterolytic cleavage.
(a) CH3 – SCH3 (b) CH3 – CN (C) CH3 – Cu


The curved-arrow notation of the given compound:



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Discuss short and convenient method (bond line notations) of representing organic molecules ?


In these notations, the bonds are represented  by lines and carbon atoms by line ends and intersections. For example. 
(i) n-Hexane may be represented as:



(ii) 2-Methylbuta-1, 3-diene may be represented as:



(iii) Hexa -1, 3, 5-triene may be represented as:

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