Concept explainers
Interpretation:
The IUPAC names of the given compounds are to be written.
Concept introduction:
In chemical nomenclature, the
The parent chain is the longest continuous chain of carbon atoms.
The parent chain is numbered from that end, which is closest to the substituent.
If the same substituent occurs more than once, the location of each point on which the substituent occurs is given.
If there are two or more different substituents they are listed in alphabetical order using the base name
The name of the alkane is derived from the parent chain with a prefix of the substituent along with their position on the chain.
For naming the cyclic organic compounds, the word “cyclo” is used as prefix.
For
The branched chain
The lengthiest continuous chain of carbon atoms is to be found for the parent name of the given alkane. For two equal chains, the chain that has more substituents will be selected.
The parent chain is to be numbered in such a way that a substituent gets the minimum possible number. For equal branching from both ends of the chain, the substituent is to be numbered such that their sum is the least.
Each of the given substituents should be numbered according to its position in the parent chain and then it should be listed in the alphabetical order. For two substituents on the same carbon, the number is repeated twice for the two substituents.
For identical substituents, a prefix is used for the number of substituents.
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Chapter 4 Solutions
ORGANIC CHEMISTRY (LL) W/WILEYPLUS NEXT
- Identify the missing organic reactants in the following reaction: X + Y H+ two steps Note: This chemical equation only focuses on the important organic molecules in the reaction. Additional inorganic or small-molecule reactants or products (like H2O) are not shown. In the drawing area below, draw the skeletal ("line") structures of the missing organic reactants X and Y. You may draw the structures in any arrangement that you like, so long as they aren't touching. Click and drag to start drawing a structure. Х :arrow_forwardDraw the mechanism of friedel-crafts acylation using acetyl chloride of m-Xylenearrow_forwardI need help naming these in IUPACarrow_forward
- H R Part: 1/2 :CI: is a/an electrophile Part 2 of 2 Draw the skeletal structure of the product(s) for the Lewis acid-base reaction. Include lone pairs and formal charges (if applicable) on the structures. 4-7: H ö- H Skip Part Check X :C1: $ % L Fi Click and drag to start drawing a structure. MacBook Pro & ㅁ x G 0: P Add or increase positive formal cha Save For Later Submit ©2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centearrow_forwardDraw the friedel-crafts acylation mechanism of m-Xylenearrow_forwardDon't used hand raiting and don't used Ai solutionarrow_forward
- 1. Base on this experimental results, how do you know that the product which you are turning in is methyl 3-nitrobenzoate(meta substituted product ) rather than either of the other two products? 2. What observation suggests that at least a small amount of one or both of the other two isomers are in the mother liquor?arrow_forwardExplain Huckel's rule.arrow_forwardhere is my question can u help me please!arrow_forward
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