Draw the skeletal structure of (S)-3-bromo-3- iodohexane. Use a dash or wedge bond to indicate the relative relationship of substituents, where applicable. Drawing
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- Draw a skeletal (line-bond) structure of trans-1,3- dimethylcyclohexane. Use a dash or wedge bond to indicate the relative relationship of substituents , where applicable .HO₂ H COOH COOH V POH HOT COOH cooff VI Ho HO COOH COOH VI H H COOH COOH VIIL OH OH Question: In the structures / examples abovke Identify V, VI, VII and VIII as Identical enantiomers, ciastereomes, stereo/cumers and/or structural isomers (there are 6 pairs 7 Comp eand to discover te I&T I TEN TEM TIMIN).Draw the skeletal structure of (R)-2-bromo-4- ethylhexane. Use a dash or wedge bond to indicate the relative relationship of substituents, where applicable. Drawing
- Please don't provide handwritten solution ....The skeletal line formula for a branched alkene is shown below. (i) What is the molecular formula of this compound? (ii) How many carbon atoms are in the longest chain, ignoring the double bond? (iii) What is the longest chain incorporating both carbons of the double bond? (iv) How many substituents are on this chain? (v) Give the IUPAC name for this compound. [6]Draw a resonance structure, complete with all formal charges and lone (unshared) electron pairs, that shows the resonance interaction of the cyano with the ortho position in benzonitrile. CEN benzonitrile • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • In cases where there is more than one answer, just draw one.
- 2. Draw structures for each of the following (a) cis-2,3-Dichloro-2-hexene (b) trans-2-burene © 1,3-dimethylcyclohexeneDraw Newman projections for the anti, eclipsed, gauche and fully eclipsed conformations of Butane. Indicate their relative stabilities and the reasons for your ranking-need to discuss the stresses involved in each case. Using suitable specific conformers of specific structures as examples, explain the difference between (a) angle strain (b) torsional strain and (c) steric strain. Need to draw the confomers and structures 4) Draw the most stable conformers using chair structures of the following: (c) cis-1,2-Dibromocyclohexane (d) trans-1,2-Dibromocyclohexane (e) cis-Decalin (f) trans-Decalin . Draw the most stable conformers of trans-1-Bromo-4-methylcyclohexane and cis-1-Bromo-4-methylcyclohexane. Which is more stable? Explain the reason for your answer. Need to include a discussion of 1,3-Diaxial interactionMembers of this series are not as chemcially reactive as the other hydrocarbons, and each has a higher molecular weight as a result of an additional -CH_2_. (That's suppose to be a small two) A) hydrocarbon B) polymer C) alcohol D) paraffin Can you help me understand which one it is please?!
- Please don't provide handwritten solution .....Quiz: Exam 3 (Final) -> A ilearn.laccd.edu/courses/132371/quizzes/939964/take/questions/2012.. Fill in the blanks: The name for is Cl The name for is The common name for is H,C HO The common name for is Br The name for isExamine the ungraded ball-and-stick model to determine the three-dimensional structure of the molecule. On the corresponding 2D structure, draw one wedge bond and one dash bond over two existing bonds to indicate the same arrangement of atoms in space. The narrow part of each wedge-and-dash bond should be towards the same central carbon atom. Click on the three-dimensional molecular structure of (S)-1-chloro-2,3-dimethylbutane and drag to rotate it, or use the controls provided. 80 F3 $ 4 R F 000 COD F4 D V % 5 C T G MA F5 B OH 6 CL MacBook Pro Y Fo H & 7 N da F7 U * 00 8 M DII FO - Change two bonds to stereobonds. K Select Draw Rings More ////// 3 ( 9 H CH₂ */ CH₂ G DD F9 H O V H,C ) O command F10 P A C - H F11 Q2Q Cl { option + = F12 Erase = ] (1) dele