I drewed all stereoisomers of 1-bromo-2-chlorocyclohexane, but it saying please indicate the orientation of the Cl...
Draw all stereoisomers of 4-bromo-2-pentene. Position the groups attached to the double bond (120° bond angles) to indicate its stereochemistry. Don't use bold wedges,hashed wedges, or wavy or criss-cross bonds to indicate double-bond stereochemistry. Do use bold and hashed wedges to indicate the configuration at C(sp3)stereocenters.*please help!!
If appropriate, please include multiple stereoisomers with the appropriate dashes and wedges. Thanks! Predict the major organic product for the following multistep sequence. Be sure your answer accounts for stereochemistry and regiochemistry, where appropriate. If multiple stereoisomers are formed, be sure to draw all products using appropriate wedges and dashes. Ha CH3 1. H C 2. H30+ Нас CH3 Ph CH3 3. Ph
please answer all questions. 3. Draw all possible stereoisomers of 2-isopropylcyclobutanamine. Use solid and dashed wedges, where appropriate. (2 pts) NH2 2-isopropylcyclobutanamine Provide (RS)-designations for the four starred (*) chiral (stereogenic) centers. (2 pts) 4. II . I I NT CH3
please i need help with all questions.. thanks Assign formal charges to all atoms in the following Lewis diagrams. (a) (b) (d) (c) : Br: 0 of H -Br: : A pt :: :0: F: Br: pt Cl pt As 1 pt hydroxyl O Br doubly bonded O F 1 pt terminal O S singly bonded O 1 pt H 1 pt on all the atoms in the following Lewis diagrams. Determine the formal charges t B N- pt N-0-...
Please put all 6 steps. Design a synthesis of 2-bromo-1-chloro-4-nitrobenzene from benzene or any mono-substituted benzene. Cl Br benzene or any mono-substituted benzene NO2 Part 1 out of 6 Choose the best option for the immediate precursor to the target molecule. CI Br NO2
please answer this question as soon as possible Q11. The correct structure of trans-1-bromo-3-methyl cyclopentane is Br (A) (B) -Br Br (C) (D) Br Q12. The correct order of increasing stability for the following conformations is СН3 H H. H H H H CH,CHZ H H СН3 H CH2CH3 CH3 CH3CH2 H2C СН3 CH3 II (B) I < III <II (A) III < II <I (C) II <I<III (D) I<II < III
These are all the answers I have tried that are wrong. Review Part A A ring with radius R and a uniformly distributed total charge Qlies in the xy plane, centered at the origin. (Figure 1) What is the potential V(z) due to the ring on the z axis as a function of z? Express your answer in terms of Q, z, R, and eo or Figure 1 of 1 ATEO View Available Hint(s) 0 r.1on Submitted Answers ANSWER 1:...
please answer and label all steps Hydrolysis of 2-bromo-2-methylpropane (tert-butyl bromide) yields 2-methylpropan-2-ol. (сн), сон + н,о* + CH CBr 2H,O Br Give the SN1 mechanism. The reactants are already given in step 1; you need to start by adding curved arrow(s) to the reactants. For each remaining step, draw all species regardless of if they are involved in that step or not. Also, include electrons and charges where necessary. Details count Note: You should have 4 carbon atoms, 13...
everything is correct except for step 3 i dont know whats wrong Hydrolysis of 2-bromo-2-methylpropane (tert-butyl bromide) yields 2-methylpropan-2-ol. (CH),CBr + 2H,0 → (CH),COH + H,0* + Br Give the Sn1 mechanism. The reactants are already given in step 1: you need to start by adding curved arrow(s) to the reactants. For each remaining step, draw all species regardless of if they are involved in that step or not. Also, include electrons and charges where necessary. Details count. Note: You...