Concept explainers
Interpretation: The name of isopropyl and sec-butyl in
Concept introduction: Systematic way to name different organic compounds is
Rules for nomenclature of
1 The longest continuous carbon chain is identified first and named in accordance with the number of carbon atoms present in it. For example, hydrocarbon with one carbon atom has prefix “meth”, that with two carbon atoms has prefix “eth”, that with three carbon atoms has prefix “prop” and so on. Suffix used for alkanes is “ane.”
2. Substituents attached to the parent carbon chain are to be identified. These are named by removal of single hydrogen atom from carbon chain end and named by replacement of suffix “ane” by “yl.” For example if
3. Carbons of the parent chain are named in such a way that substituents acquire the lowest numbers.
4. If same substituent is present more than one time in the molecule, it is represented by prefix “di”, “tri” and so on. It depends on number of times substituent occurs in molecule.
5. If two or more substituents are present in the molecule, these are named in alphabetical order.
6. If carbon chains of same length exist in the same molecule, chain with the largest number of side chains, followed by lowest number to substituents, chain with the greatest number of carbon atoms in smaller chain and chain with the least branched side chains are preferred over other ones.
7. Prefix “cyclo” is used if cyclic alkane is present in the molecule.
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Chapter NW1 Solutions
Custom eBook for Organic Chemistry
- Show work with explanation. Don't give Ai generated solutionarrow_forwardShow work. don't give Ai generated solutionarrow_forwardUse the average molarity of acetic acid (0.0867M) to calculate the concentration in % (m/v). Then calculate the % difference between the calculated concentrations of your unknown vinegar solution with the 5.00% (w/v%) vinegar solution (check the formula for % difference in the previous lab or online). Before calculating the difference with vinegar, remember that this %(m/v) is of the diluted solution. It has been diluted 10 times.arrow_forward
- #1. Retro-Electrochemical Reaction: A ring has been made, but the light is causing the molecule to un- cyclize. Undo the ring into all possible molecules. (2pts, no partial credit) hvarrow_forwardDon't used Ai solutionarrow_forwardI have a question about this problem involving mechanisms and drawing curved arrows for acids and bases. I know we need to identify the nucleophile and electrophile, but are there different types of reactions? For instance, what about Grignard reagents and other types that I might not be familiar with? Can you help me with this? I want to identify the names of the mechanisms for problems 1-14, such as Gilman reagents and others. Are they all the same? Also, could you rewrite it so I can better understand? The handwriting is pretty cluttered. Additionally, I need to label the nucleophile and electrophile, but my main concern is whether those reactions differ, like the "Brønsted-Lowry acid-base mechanism, Lewis acid-base mechanism, acid-catalyzed mechanisms, acid-catalyzed reactions, base-catalyzed reactions, nucleophilic substitution mechanisms (SN1 and SN2), elimination reactions (E1 and E2), organometallic mechanisms, and so forth."arrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning
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