Using the templates provided, draw the planar representation (use wedges and dashes!) and both chair conformations...
Using the templates provided, draw the planar representation (use wedges and dashes!) and both chair conformations of the models of 1,2-dichlorocyclohexane in the table below Is one chair conformer lower in energy? If so, circle the appropriate conformer(s) above. Are the two chlorine atoms cis- or trans- to each other? Can both chlorine atoms be axial in any chair conformation? 72
Build two models of chlorocyclohexane... help with answers! 4. Build two models of chlorocyclohexane. On one model, replace the hydrogen labeled H, with a chlorine atom to make model A; on the other model, replace the hydrogen labeled H, to produce model B. Now place both models in the chair conformation. H model A replace H B H H СІ H H replace H. mandel What is the configuration of each chirality center? A? RS B? RS C? RS D?...
or trans where approprium or stereoisomers. 5. Using only chair conformations, make and draw molecular models for all of the 1.4. dibromocyclohexanes. Clearly indicate which are related as conformational isomers and which are related as configurational isomers. Designate the configurational isomers as cis or trans. Explain which isomers equilibrate rapidly with each other interconvert). 6. Draw the two chair conformations of trans-1,4-dichlorocyclohexane. Construct a qualitative plot (reaction energy diagram) that describes the energy of the system as a function of...
ich has the highest energy? 7. a) Depending upon the kind of models you are using, you may or may not be able to construct models of cyclopropane and cyclobutane. Do so, if possible, but do not break the linkages. Why do we say that these molecules are strained? What is the normal sp3 bond angle? What are the (internal) C-C-C bond angles in cyclopropane? b) Make a model of cyclopentane. Does this molecule seem to have any ring strain...