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- Draw the structures of the following molecules: (a) trans-l-Bromo-3-methylcyclohexane (b) cis-1, 2-Dimethylcyclobutane (c) trans-1 -tert-Butyl-2-ethylcyclohexaneWrite the complete common (not IUPAC) name of each molecule below. Note: if a molecule is one of a pair of enantiomers, be sure you start its name with D- or L- so we know which enantiomer it is. molecule i H3N + NH3 common name (not the IUPAC name) H N NH ☐ شهدة + NH3 | ☑Write the complete common (not IUPAC) name of each molecule below. Note: if a molecule is one of a pair of enantiomers, be sure you start its name with D- or L- so we know which enantiomer it is. molecule H₂N NH3 NH3 S. common name (not the IUPAC name) 0 0 1
- Write the complete common (not IUPAC) name of each molecule below. Note: if a molecule is one of a pair of enantiomers, be sure you start its name with D- or L- so we know which enantiomer it is. molecule NH3 common name (not the IUPAC name) H NH ☐ H3N 0 NH3 مل xName the alkene. Be sure to indicate stereochemistry and use hyphens (-) not endashes (-). H₂C-CH₂ H H₂C H₂C-HC C=C The alkene is named: H CH3Write de complete (not UIPAC) name of each molecule below. Note: If a molecule is one of a pair of enantiomers, be sure you start its name with D- or L- so we know which enantiomer it is. molecule H₂N H₂N. HS NH3 NH3 common name (not the IUPAC name) 0 0
- Please identify the relationship between each pair of structures as: (i) identical, (ii) constitutional, (iii) conformational, (iv) enantiomers, or (v) diastereomers. Choose only one label per pair of structures.Please explain completely and give IUPAC name according to rules and NumberingDoes the molecule below exist as a pair of enantiomers? If so, change the bonds to wedges and dashes to reflect S stereochemistry. If the molecule does not exist as a pair of enantiomers, check the box below. O Does not exist as enantiomers H Br 0 X
- 2 1 Group activity: Use molecular model to convert the given 3D perspective structure to Newman projection around C-C bond on the template provided. Fill in the substituent for the most stable conformation in the templates provided. H H OH Br OH CH Y/ 3D of most stable conformation ΕΙ Fischer projection of most stable conformation most stable conformation Use the molecular model of chair conformation of cyclohexane and fill in the substituents in the template provided for chair conformation and complete the Newman projections showing only substituents for given molecules. Circle the chair conformation which is more stable. 1) cis-3-isopropylcyclohexanol 2) trans-3-Isopropylcyclohexaol QODraw the structure for meso-1,3-dimethylcyclohexane. Be sure to indicate stereochemistry using wedge and dashed bonds. Click and drag to start drawing a structure. D с с X S J (x èAnswer the following questions based on these structures. Here is the terminology you can use to describe the relationships. Structural isomers, Enantiomers, Diastereomers, and no relationship. CHO CHO -Н H- I CHO HO-H H- -OH -OH CH₂OH 1 I НО- OH I I CHO -H H -ОН -ОН HO I CH₂OH =0 H -OH CH₂OH 2 H H но Но CHO НО H H НО -ОН -ОН -H -H CH2OH 8 -H OH OH H CH₂OH 3 I НО CH₂OH 7 What is the relationship between 1 and 4? What is the relationship between 1 and 3? What is the relationship between 1 and 5? What is the relationship between 2 and 9? What is the relationship between 4 and 10? What is the relationship between 5 and 6? What is the relationship between 2 and 10? CH2OH -ОН -Н CH2OH 9 НО H- H CH2OH 0 H -ОН ОН CH2OH Н- НО- НО- НО НО H- Н- CH2OH -0 -ОН -H -H CH2OH 10 H -OH ОН CH2OH 5 Н НО НО- H- CHO OH -Н H OH CH₂OH 6