Concept explainers
Interpretation:
Newman projection for the given compound and IUPAC name has to be provided.
Concept Introduction:
Nomenclature of organic compounds:
The naming of the organic compound is given by IUPAC (International Union for pure and applied chemistry). In the IUPAC names consist of certain rules for giving chemical names they are,
- The longer number of Carbon chain of a compound is identified this is called parent of the compound.
- In the cyclic compounds the number of carbon involving in ring formation is called parent of the compound.
- The compound have more than one parent chains means the larger number of substitutions present in the chain is consider as a parent chain.
- The names of all substituents are arranged by alphabets to starts with lowest numbering.
- The complex substituent is built by a substituent on a substituent; so called complex substituent.
- In the complex substituent having compounds the substituent name is assigned by a name each of them based on numbers going away from the parent.
Conformations: Rotation about C-C single bonds allows a compound to adopt a variety of possible three-dimensional shapes.
Newman projections: The new conformations of compounds can be drawn and analyzed by Newman projections. A Newman projection visualizes different conformations of Carbon-carbon
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Chapter 4 Solutions
ORGANIC CHEMISTRYPKGDRL+MLCRL MDL
- Which of the following molecules are NOT typical carbohydrates? For the molecules that are carbohydrates, label them as an aldose or ketose. HO Он ОН ОН Он ОН но ΤΗ HO ОН HO eve Он он ОН ОН ОН If polyethylene has an average molecular weight of 25,000 g/mol, how many repeat units are present?arrow_forwardDraw the a-anomer cyclized pyranose Haworth projection of the below hexose. Circle the anomeric carbons. Number the carbons on the Fischer and Haworth projections. Assign R and S for each chiral center. HO CHO -H HO -H H- -OH H -OH CH₂OH Draw the ẞ-anomer cyclized furanose Haworth projection for the below hexose. Circle the anomeric carbons. Number the carbons on the Fischer and Haworth projections. HO CHO -H H -OH HO -H H -OH CH₂OHarrow_forwardName the below disaccharide. Circle any hemiacetals. Identify the numbering of glycosidic linkage, and identify it as a or ẞ. OH HO HO OH HO HO HO OHarrow_forward
- What are the monomers used to make the following polymers? F. а. b. с. d. Вецер хочому なarrow_forward1. Propose a reasonable mechanism for the following transformation. I'm looking for curved mechanistic arrows and appropriate formal charges on intermediates. OMe MeO OMe Me2N NMe2 OTBS OH xylenes OMe 'OTBSarrow_forwardWhat is the polymer made from the following monomers? What type of polymerization is used for each? а. ОН H2N но b. ن -NH2 d. H₂N NH2 довarrow_forward
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- Which representation(s) show polymer structures that are likely to result in rigid, hard materials and those that are likely to result in flexible, stretchable, soft materials?arrow_forward3. Enter the molecular weight of the product obtained from the Williamson Ether Synthesis? OH OH & OH excess CH3l Ag₂Oarrow_forwardPlease answer 1, 2 and 3 on the endarrow_forward
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