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(a)
Interpretation:
The structure of an amide with formula
Concept Introduction:
Amide: One
Depending on the number of carbon side chain of the amide, different types of amides can form.
(b)
Interpretation:
The structure of an
Concept Introduction:
Functional group: They are certain substitutes in the organic molecules which are determine the characteristic reactions taking place in it.
Aldehyde: One alkyl group and a hydrogen atom are attached to the carbonyl carbon atom of the compound. It is represented as
(c)
Interpretation:
The structure of an aromatic compound which is an ether with molecular formula
Concept Introduction:
Functional group: They are certain substitutes in the organic molecules which are determine the characteristic reactions taking place in it.
Ether: Ether is a group of organic compound where two aryl or alkyl groups are connected by an oxygen atom. It is represented as
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Chapter 12 Solutions
Fundamentals of General, Organic, and Biological Chemistry (8th Edition)
- Draw the product of this reaction. Ignore inorganic byproducts. HO C=0 H ⚫OH H ⚫OH HO- H HO H CH2OH Tollens' solution Draw Fischer Projectionarrow_forwardDraw the product of this reaction. Ignore inorganic byproducts. H-C=O HO H HO H H- ⚫OH HO H CH2OH HNO3, H2O Draw Fischer Projectionarrow_forwardDraw the product of this reaction. Ignore inorganic byproducts. HO HO- HO H HO ∙H HO CH2OH NaBH4, CH3OH Draw Fischer Projectionarrow_forward
- Draw the product of this reaction. Ignore inorganic byproducts. Но сво HO H HO H H OH H -OH CH2OH H2 Pd Draw Fischer Projectionarrow_forwardDraw the Haworth projection for Gulose-ẞ-1,6-sorbose and answer the following questions. (Gulose will be in the pyranose form and Sorbose will be in the furanose form) a. Label the reducing and nonreducing ends of the disaccharide b. Label the glycosidic bond c. Circle the anomeric carbons and label them as hemiacetals or acetals. d. Can this disaccharide undergo mutarotation?arrow_forwardDraw the product of the reaction below. Ignore inorganic byproducts. H OH HO HO HO ·H H OH H OH excess CH3CH2I KOHarrow_forward
- Draw the Haworth structures for the following: a. α-D-Gulopyranose b. ẞ-D-Sorbofuranose c. The two possible isomers of a-D-altrose (furanose and pyranose forms)arrow_forwardDraw the product of this reaction. Ignore inorganic byproducts. HO H ⚫OH HO- ∙H H- -OH H ⚫OH CH2OH HNO3, H2Oarrow_forwardDraw the product of the reaction below. Ignore inorganic byproducts. HO CH2OH OH OH OH excess CHзI Ag2Oarrow_forward
- Draw the product of the reaction below. Ignore inorganic byproducts. HOH HO H -OAC H OH OH H excess CHзI Ag2Oarrow_forwardDraw the product of this reaction. Ignore inorganic byproducts. H- H ⚫OH HO H H- OH H ⚫OH CH2OH NaBH4, CH3OHarrow_forwardDraw B-D-galactopyranose and ẞ-D-mannopyranose in their chair conformations. Label the axial and equatorial positions.arrow_forward
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