When do we use the prefixes iso, neo, tert, sec when we name organic compounds?
Answer
546.6k+ views
Hint: the names of organic compounds follow the IUPAC nomenclature, but sometimes for ease, we follow common names of organic compounds which are different from IUPAC names. The common consist of some prefixes which indicates the spatial arrangement of functional groups (usually alkyl substitutions)
Complete answer:
The prefix "iso" is used when all carbons except one form a continuous chain. The prefix "neo" is used when all but two carbons form a continuous chain. The prefix "sec" or "s" is used when the functional; group is bonded to a secondary carbon (although this can be used only for the chain containing four or more carbons). The prefix "tert" or "t" is used when the functional group is bonded to a tertiary carbon.
For example, the first structure is normal pentane, the second is isopentane and the third represents the neopentane, these follow the criteria for the prefixes.
Now, the following structures represent the sec and tert butanol. The first structure is sec butanol and the second structure is tert butanol. In the first one, the functional group is attached to secondary carbon (carbon attached to two carbon atoms) and in the second structure, the functional group is attached to tertiary carbon atoms (carbon atoms attached to three carbon atoms).
Note:
The structure should be made carefully following the valency of carbon. Sometimes, these prefixes are also allowed to be used in the IUPAC names, for example,
5-(1-ethyl-1-isopropyl)nonane.
Complete answer:
The prefix "iso" is used when all carbons except one form a continuous chain. The prefix "neo" is used when all but two carbons form a continuous chain. The prefix "sec" or "s" is used when the functional; group is bonded to a secondary carbon (although this can be used only for the chain containing four or more carbons). The prefix "tert" or "t" is used when the functional group is bonded to a tertiary carbon.
For example, the first structure is normal pentane, the second is isopentane and the third represents the neopentane, these follow the criteria for the prefixes.
Now, the following structures represent the sec and tert butanol. The first structure is sec butanol and the second structure is tert butanol. In the first one, the functional group is attached to secondary carbon (carbon attached to two carbon atoms) and in the second structure, the functional group is attached to tertiary carbon atoms (carbon atoms attached to three carbon atoms).
Note:
The structure should be made carefully following the valency of carbon. Sometimes, these prefixes are also allowed to be used in the IUPAC names, for example,
5-(1-ethyl-1-isopropyl)nonane.
Recently Updated Pages
Write structures of the following compounds i 2 Chloro3methylpentane class 11 chemistry CBSE

What is BLO What is the full form of BLO class 8 social science CBSE

Explain the Treaty of Vienna of 1815 class 10 social science CBSE

A Paragraph on Pollution in about 100-150 Words

XIX+XXX A 49 B 51 C 55 D 44 class 5 maths CBSE

If x a + bt + ct2 where x is in meters and t is in class 11 physics CBSE

Trending doubts
One Metric ton is equal to kg A 10000 B 1000 C 100 class 11 physics CBSE

Find the value of the expression given below sin 30circ class 11 maths CBSE

What do you mean by retardation What is its SI uni class 11 physics CBSE

Draw a diagram of nephron and explain its structur class 11 biology CBSE

10 examples of friction in our daily life

Difference between physical and chemical change class 11 chemistry CBSE

