and and 2. Draw a structure for a molecule not shown in this activity that Exercises:...
Exercises: 1. Indicate if the following pairs of structures are identical, conformers, geometric isomers, constitutional isomers, or not isomers. a. 1,2-dimethylcyclobutane and 1,3-dimethylcyclobutane and and and and and - and and
Critical Thinking Questions: 12. Label one box in Model 4 with the name "dis-1,2-dimethylcyclobutane" and the other with the name "trans-1,2-dimethylcyclobutane." Then add perspective representations into each box. 13. Draw wedge-and-dash and perspective representations of cis- and trans-1,3- dimethylcyclobutane. (Note: that is "1,3-dimethyl, not "1,2-dimethyl.") Do not answer this question Exercises: 1. Indicate if the following pairs of structures are identical, conformers, geometric isomers, constitutional isomers, or not isomers. a. 1,2-dimethylcyclobutane and 1,3-dimethylcyclobutane b. and Y 2 Draw a structure...
1. Which of the following is a correct resonance structure for compound shown in the right? NH 2. What is the relationship between the following compounds? A. constitutional isomers B. resonance structures C. conformers D. identical compounds
Which is a correct resonance structure of the molecule given below? 1 2 3 4 What is the relationship between these two structures? Identical Constitutional Isomers Resonance Structures
For each molecule/ion shown, please draw the Lewis structure and indicate the formal charge on each atom. If equivalent structures exist, draw all possible "best structure" resonance structures. 1. PO. 2. Na CO 3. HCO 4. SCN- (draw 3 "best" resonance structures here)
7,8 1.1 pt) A. Designate the content e configuration of each stereoisomer for each molecule. in the phenstructures as Ror 5 B. Draw indicated OH enantiomer diastereomer 8.1 p.) identify the specific type of relationship between each of the following pairs of molecules (le, either the same, constitutional isomers, enantiomers, diastereomers, conformers or unrelated)
Draw three-dimensional depictions of the following molecules. For each molecule provide theoretical bond angles, shape, and electron group geometry (ie octahedral, tetrahedral, bent, etc.). For each molecule, provide all possible structural and geometric isomers. If the molecule/ion possesses resonance structures, draw all relevant structures? What is the point group of each structure? If the compound is chiral, draw its enantiomer. NiCl2(NH3)2 (tetrahedral) PCl2F3 NO3-
7) How many enantiomers are there of the molecule are there of the molecule shown bole CO2H 1 1 OH 1 CH2OH A) B)1 C)2 D) 3 E) 6 8) What term describes the structural relationship between (2R 3R.45)-2.3.4-trichloroheptane and (2S,3S,4R)-2,3,4-trichloroheptane? A) not isomers B) constitutional isomers C) enantiomers D) diastereomers E) conformers 9) Label cach asymmetric carbon in the molecule below as having the Ror S configuration. A) 1R, 2R B) IR, 2S C) IS, 2R D) IS, 2S...
1. Draw the structure of n-pentane and all of its constitutional isomers. 2. Draw (showing stereochemistry) the meso isomer of 2,3-dibromobutane. 3. Draw two examples of cis-trans isomers with the molecular formula C6H12, one pair containing a double bond and pair containing a ring. (Four structures in total)
1. Identify all the chiral centers in the y all the chiral centers in the molecule below: 2. For each of the pairs of compounds, de indicate if they are identical, enantiomers, diastereomers, constitutional isomers or different compounds. 3. Identify the chiral centers in the diastereomers below and label each as R or S.