Concept explainers
Interpretation: Whether the answers in CTQ are in agreement with Memorization Task NW1.2 given below or not should be given.
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 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 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 parent chain are named in such way that substituents acquire the lowest numbers.
4. If same substituent is present more than one time in 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 molecule, these are named in alphabetical order.
6. If carbon chains of same length exist in 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 molecule.
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Check out a sample textbook solutionChapter NW1 Solutions
Organic Chemistry: A Guided Inquiry
- Organic Functional Groups Identifying positions labeled with Greek letters in acids and derivatives If possible, replace an H atom on the a carbon of the molecule in the drawing area with a methyl group substituent, and replace an H atom on the ß carbon with a hydroxyl group substituent. If one of the substituents can't be added for any reason, just don't add it. If neither substituent can be added, check the box under the drawing area. HO Oneither substituent can be added. OH 0/5 Xarrow_forwardUse the IUPAC Nomenclature System to name the following ester: CH₂ | CH,—CH–CH,-C-O-CH, X 5arrow_forward(E) What suffix do all the names in Model 1 have in common with each other?arrow_forward
- Use Model 1 to propose names for three-, four-, five-, and six-carbon branches that follow the same pattern as “methyl” and “ethyl” for one- and two-carbon branches, respectively. (Note: The names of seven-, eight-, etc. carbon branches follow the same pattern, but branches of such length are rare since they are usually the parent chain.)arrow_forward3. Use curved arrows to show electron movement in the reactant side and draw the product/s of the Lewis (nucleophile-electrophile) reaction. Draw in all lone pairs and charges where appropriate. acid-base -co +arrow_forward7. Draw curved arrows indicating the movements of electrons between the following pair of resonance structures. Name the pattern of resonance shown. What is the hybridization of the carbon atoms? 8. Draw the remaining three resonance structures for the molecule in problem 7 above. 9. There are several possible forms of a trisubstituted cyclohexane with the formula C10H200. I have drawn four of them. From these, which one do you think is most commonly naturally occurring, and why? Which is least commonly occurring and why? HO HO" HO HOarrow_forward
- Hi ! Can you please explain how this organic molecule would have a Z configuration? Thanksarrow_forwardComplete the following statements so that they are true. Ry value. Ry value. R; value. Ry value. a. A more polar compound has a b. A less polar compound has a c. A more polar solvent causes a d. A less polar solvent causes a e. To increase the Ry of a spot, you should add more of which solvent, hexanes or ethyl acetate?arrow_forward1. Draw ethylbenzene and put a + on the carbon next to the benzene (innermost carbon in ethyl group). Show all resonance forms for this ion. 2. draw the naphthalene and put one - on the neighboring carbon of the "crossroads". show every resonance forms for this ion. 3. Draw benzoic acid and draw on all p-orbitals.arrow_forward
- Organic Chemistry: A Guided InquiryChemistryISBN:9780618974122Author:Andrei StraumanisPublisher:Cengage Learning