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Concept explainers
(a)
Interpretation:
The structure of the incorrectly named compound should be determined along with the correct name of the compound.
2-ethyl-3-methyl-5-isopropyl hexane
Concept Introduction:
Compounds consist of carbon and hydrogen is known as hydrocarbons.
Rules of naming saturated and
- First choose the longest continuous chain of carbon atoms known as parent chain.
- The numbering of parent chain should be done in a way that the substituents, double bond and triple bond get the lowest number.
- In case of
alkene , “ene” is used at the end of the name and in case ofalkyne , “yne” is used at the end of the name. - The appropriate name should be given to every alkyl group and denote its position on the parent chain with the number.
- The alkyl groups are written in alphabetical order.
(b)
Interpretation:
The structure of the incorrectly named compound should be determined along with the correct name of the compound.
3-methyl-4-isopropyl pentane
Concept Introduction:
Compounds consist of carbon and hydrogen is known as hydrocarbons.
Rules of naming saturated and unsaturated hydrocarbons are:
- First choose the longest continuous chain of carbon atoms known as parent chain.
- The numbering of parent chain should be done in a way that the substituents, double bond and triple bond get the lowest number.
- In case of alkene, “ene” is used at the end of the name and in case of alkyne, “yne” is used at the end of the name.
- The appropriate name should be given to every alkyl group and denote its position on the parent chain with the number.
- The alkyl groups are written in alphabetical order.
(c)
Interpretation:
The structure of the incorrectly named compound should be determined along with the correct name of the compound.
2-ethyl-3-butyne
Concept Introduction:
Compounds consist of carbon and hydrogen is known as hydrocarbons.
Rules of naming saturated and unsaturated hydrocarbons are:
- First choose the longest continuous chain of carbon atoms known as parent chain.
- The numbering of parent chain should be done in a way that the substituents, double bond and triple bond get the lowest number.
- In case of alkene, “ene” is used at the end of the name and in case of alkyne, “yne” is used at the end of the name.
- The appropriate name should be given to every alkyl group and denote its position on the parent chain with the number.
- The alkyl groups are written in alphabetical order.
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Chapter 20 Solutions
Introductory Chemistry: A Foundation
- Can you please help me with this problem and explain it step by step? I'm so confused about itarrow_forward2. Identify the reagents you would need to achieve the following. You may need to consider using a protecting group. HO 1. 2. 3. 4. 5. OH Br HOarrow_forwardBeF2 exists as a linear molecule. Which kind of hybrid orbitals does Be use in this compound? Use Orbital Diagrams to show how the orbitals are formed. (6)arrow_forward
- Please answer the questions and provide detailed explanations as well as a drawing to show the signals in the molecule.arrow_forwardPropose an efficient synthesis for the following transformation: EN The transformation above can be performed with some reagent or combination of the reagents listed below. Give the necessary reagents in the correct order, as a string of letters (without spaces or punctuation, such as "EBF"). If there is more than one correct solution, provide just one answer. A. t-BuOK B. Na2Cr2O7, H2SO4, H2O C. NBS, heat F. NaCN D. MeOH E. NaOH G. MeONa H. H2O I. 1) O3; 2) DMSarrow_forwardStereochemistry Identifying the enantiomer of a simple organic molecule 1/5 Check the box under each structure in the table that is an enantiomer of the molecule shown below. If none of them are, check the none of t above box under the table. Br ま HO H 0 Molecule 1 Molecule 2 Molecule 3 OH H Br H H" Br OH Br Molecule 4 Br H OH + + OH Molecule 5 Br H OH none of the above Molecule 6 Br H... OHarrow_forward
- Please answer the questions and provide detailed explanations.arrow_forwardQuestion 16 0/1 pts Choose the correct option for the following cycloaddition reaction. C CF3 CF3 CF3 CF3 The reaction is suprafacial/surafacial and forbidden The reaction is antarafacial/antarafacial and forbidden The reaction is antarafacial/antarafacial and allowed The reaction is suprafacial/surafacial and allowedarrow_forward1. Give the structures of the products obtained when the following are heated. Include stereochemistry where relevant. A NO2 + NO2 B + C N=C CEN + { 2. Which compounds would you heat together in order to synthesize the following?arrow_forward
- Explain how myo-inositol is different from D-chiro-inositol. use scholarly sources and please hyperlink.arrow_forwardWhat is the molarisuty of a 0.396 m glucose solution if its density is 1.16 g/mL? MM glucose 180.2 /mol.arrow_forwardProvide the proper IUPAC or common name for the following compound. Dashes, commas, and spaces must be used correctly. Br ......Im OHarrow_forward
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