For each compound, mark the stereocenter (if any) with an asterisk, tell whether the molecule is chiral or achiral, and tell how many stereoisomers are possible.
Tetrahedral carbon (sp3 hybridized) attached to 4 different groups (or) atoms will be chiral carbon.
For each compound, mark the stereocenter (if any) with an asterisk, tell whether the molecule is...
Highlight, by clicking on, the asymmetric carbons (if any) in each structure. A selected atom l turn green. Cl CH2 CH3 H3C Indicate whether each compound is chiral and the number of stereocenters (see Hint) in each molecule. □ achiral □ chiral □ no stereocenters □ one stereocenter □ two stereocenters □ three stereocenters □ achiral □ chiral □ one stereocenter □ three stereocenters no stereocenters two stereocenters
1.A. Place an asterisk (*) next to each stereocenter of these four compounds. 1.3. Bubble in if the compound is chiral or achiral. 1.C. Determine the stereochemical relationship between each possible pair. Br Br Br Br A B D chiral O achiral OO chiral achiral с Ochiral achiral 8 chiral achiral A and B: 000 identical enantiomers diastereomers none of these A and C: ооо identical enantiomers O diastereomers none of these A and D: оооооо O identical enantiomers diastereomers...
Highlight, by clicking on, the asymmetric carbons (if any) in each structure. A selected atom will turn green. Indicate whether each compound is chiral and the number of stereocenters (see Hint) in each molecule achiral chiral no stereocenters one stereocenter two stereocenters three stereocenters achiral chiral no stereocenters one stereocenter two stereocenters three stereocenters
(6 points) Place an asterisk (*) next to each stereocenter in the following molecule. 8. OH Br How many stereoisomers are possible for this molecule? Inrimary Secon
2. Mark all stereocenters with an asterisk (*) and assign the configuration (R or S) for each. Also write whether the molecule is chiral, achiral, or meso (3 pts each) H CH2OH b. c. tch Br Сн, 3. Name the following compounds (2 pts each) Br b.
1. Draw the (major) organic products of the following reactions: HNO3 H2SO4 HN (CH3)3CBr AlBr3 FeBr3 Br Sort the following molecules by their reactivity toward electrophilic aromatic substitution (1-most reactive, 4 2. least reactive): NH2 so,H Place either the letter A or C below the following compounds to indicate whether each of them are achiral (A) or chiral (C) 3. но Cl Determine the configuration (R or S) for each stereocenter in the following compounds: 4. Cl Cl NH2 но...
(6 points) Place an asterisk (*) next to each stereocenter in the following molecule. 8 How many stereoisomers are possible for this molecule? 9. (8 points) Determine the molecular formula and how many primary, secondary, tertiary and quaternary carbons are present by writing the correct number next to the designation below. Molecular Formula carbons 40 2 30 How many: 1 9 HO 10. (8 points) Complete the below by drawing the structures of both products for both reactions (Ox] но...
**WRITTEN WORK** For the following molecule, label each stereocenter with an asterisk (*), and draw all possible configurational isomers. OH Br
Please Explain. (2) How many stereocenters does each molecule have. How many stereoisomers each molecule can have in theory? Br Br CI Br а от OH ОН ОН ОН (3) Circle the chiral molecules. If molecule is achiral – show its plane of symmetry. Н Н. СІ CI Br Br Br да» 2 HT / / CH3 CH3 1 1
3) (6 pts) Draw a line structure of an organic molecule that contains exactly 12 carbons, five-membered ring an nitrogen atom, an ester group and a secondary alcohol group. Number all carbon atoms. Place an asterisk (*) next to any chiral carbons that may exist in the structure and state how many stereoisomers are possible for the molecule. # of chiral carbons: # of possible stereoisomers: 4) (6 pts) Draw a line structure of an organic molecule that contains 12...