
Interpretation:
The stereochemical formulas of the products obtained for the given reactions are to be written.
Concept introduction:
Electrophiles are electron-deficient species, which has positive or partially positive charge. Lewis acids are electrophiles, which accept electron pair.
Nucleophiles are electron-rich species, which has negative or partially negative charge. Lewis bases are nucleophiles, which donate electron pair.
Substitution reaction: A reaction in which one of the hydrogen atoms of a hydrocarbon or a functional group is substituted by any other functional group is called substitution reaction.
Elimination reaction: A reaction in which two substituent groups are detached and a double bond is formed is called elimination reaction.
Addition reaction: It is the reaction in which unsaturated bonds are converted to saturated molecules by the addition of molecules.
The compounds that have the same molecular formula of atoms but the structure of the compounds are different for the positions of atoms are called isomers.
In double bond or cyclic compounds, if two same
If the two functional groups are present on the different sides of the double bond or cyclic compound, the given compound can be labeled as Trans.
Cis-trans isomerism exists in the compounds in which similar groups are present on the adjacent carbon atoms.
The molecules that are nonsuperimposable or not identical with their mirror images are known as chiral molecules.
The stereoisomers that are nonsuperimposable on each other and not mirror images of each other are known as diastereomers.
The achiral compounds in which plane of symmetry is present internally and consists of chiral centres are known as meso compounds, but they are optically inactive.
Enantiomers are stereoisomers whose molecules contain nonsuperimposable mirror images.
A chiral molecule is one that has a nonsuperimposable mirror image and an achiral molecule is one that has a superimposable mirror image.

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Chapter 8 Solutions
EBK ORGANIC CHEMISTRY
- Phenol is the starting material for the synthesis of 2,3,4,5,6-pentachlorophenol, known al-ternatively as pentachlorophenol, or more simply as penta. At one time, penta was widely used as a wood preservative for decks, siding, and outdoor wood furniture. Draw the structural formula for pentachlorophenol and describe its synthesis from phenol.arrow_forward12 Mass Spectrometry (d) This unknown contains oxygen, but it does not show any significant infrared absorption peaks above 3000 cm . 59 100- BO 40 Relative Abundance M(102) - 15 20 25 30 35 40 45 50 5 60 65 70 75 80 85 90 95 100 105 mizarrow_forwardDraw a Haworth projection of a common cyclic form of this monosaccharide: H HO H HO H HO H H -OH CH2OH Click and drag to start drawing a structure. Х : Darrow_forward
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- Take a look at this molecule, and then answer the questions in the table below it. CH2OH H H H OH OH OH CH2OH H H H H OH H H OH H OH Is this a reducing sugar? yes α β ロ→ロ no ☑ yes Does this molecule contain a glycosidic bond? If you said this molecule does contain a glycosidic bond, write the symbol describing it. O no 0+0 If you said this molecule does contain a glycosidic bond, write the common names (including anomer and enantiomer labels) of the molecules that would be released if that bond were hydrolyzed. If there's more than one molecule, separate each name with a comma. ☐arrow_forwardAnswer the questions in the table below about this molecule: H₂N-CH₂ -C—NH–CH–C—NH–CH—COO- CH3 CH CH3 What kind of molecule is this? 0= CH2 C If you said the molecule is a peptide, write a description of it using 3-letter codes separated ☐ by dashes. polysaccharide peptide amino acid phospolipid none of the above Хarrow_forwardDraw a Haworth projection of a common cyclic form of this monosaccharide: CH₂OH C=O HO H H -OH H OH CH₂OH Click and drag to start drawing a structure. : ☐ Х S '☐arrow_forward
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