
Concept explainers
Interpretation:
The bond-line formulas of the given organic compounds are to be drawn.
Concept introduction:
A bond-line formula is a way to represent a molecular structure with a line denoting a covalent bond. In an organic compound, each end point in a line represents a carbon and hydrogen is not written. Hetero-atoms are written in bond-line formula.
In cis-isomers, substituents are on the same side of the double bond.
In trans-isomers, substituents are on the opposite side of the double bond.
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
For naming the cyclic organic compounds, the word “cyclo” is used as prefix.
For

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Chapter 4 Solutions
EBK ORGANIC CHEMISTRY
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- ΗΝ, Draw Final Product C cyclohexanone pH 4-5 Edit Enamine H3O+ CH3CH2Br THF, reflux H Edit Iminium Ionarrow_forwardHow many hydrogen atoms are connected to the indicated carbon atom?arrow_forwardIdentify the compound with the longest carbon - nitrogen bond. O CH3CH2CH=NH O CH3CH2NH2 CH3CH2C=N CH3CH=NCH 3 The length of all the carbon-nitrogen bonds are the samearrow_forward
- Identify any polar covalent bonds in epichlorohydrin with S+ and 8- symbols in the appropriate locations. Choose the correct answer below. Η H's+ 6Η Η Η Η Η Ηδ Η Ο Ο HH +Η Η +Η Η Η -8+ CIarrow_forwardH H:O::::H H H HH H::O:D:D:H HH HH H:O:D:D:H .. HH H:O:D:D:H H H Select the correct Lewis dot structure for the following compound: CH3CH2OHarrow_forwardRank the following compounds in order of decreasing boiling point. ннннн -С-С-Н . н-с- ННННН H ΗΤΗ НННН TTTĪ н-с-с-с-с-о-н НННН НН C' Н н-с-с-с-с-н НН || Ш НННН H-C-C-C-C-N-H ННННН IVarrow_forward
- Rank the following compounds in order of decreasing dipole moment. |>||>||| ||>|||>| |>|||>|| |||>||>| O ||>>||| H F H F H c=c || H c=c F F IIIarrow_forwardchoose the description that best describes the geometry for the following charged species ch3-arrow_forwardWhy isn't the ketone in this compound converted to an acetal or hemiacetal by the alcohol and acid?arrow_forward
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