Use the templates to draw the indicated structures but leave off the hydrogens since they make the drawing hard to read. Br Br Br cis-1-bromo-2-methyl B trans-1-chloro-4-bromo 7
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- Which of the following substituents is a meta detector? -CN -Cl -CH2CH3 -OHAdjust the structures below to show the resulting intermediates.. Write the structure of the product formed in the below reaction and name them. Does the product have a chiral carbon? If yes, assign R and S. Does the product have an internal plane of symmetry? If so, what do you call such molecules? Show the internal plane of symmetry by drawing a line. Please answer fast I give upvote
- Could someone help me with ranking these with how reactive they would be with an SN2 reaction? Thanks :)How many stereoisomers of 2-methyl-heptan-4-ol could form? How many would you expect to form? In what ratios? (All equal?). Explain your answer Please explain clearly why the ratio is 1:1. Thank you!10.2 Complete the following reactions: Show the step-by-step process. Do not use shortcut methods. Make it as detailed as it can be. Encode (not hand-written)!
- 3. Based on the definitions of the terms below select the best classification for the following reactive species below: nucleophile; electrophile; free radical; carbocation; carboanion, electron rich species, delocalized electrons (i) CH3-: …………………………………………(ii) Br ∙ : …………………………………………. (iii) H2O : …………………………………………. (iv) CN- : ………………………………………….(v) Cl+: …………………………………………….(vi) CH3CH2+: ……………………………………..(vii) CH3∙ : …………………………………………… (viii) CH2CH2 : …………………………………………..Assign the stereochemical configuration (E or Z) for the alkene below. Show your work, indicating clearly which groups are assigned high priority (e.g., through assigning the groups numbers, circling only the high priority groups, or labeling groups as high or low).Show how HC≡CH, CH3CH2Br, and (CH3)2CHCH2CH2Br can be used to prepare CH3CH2C≡CCH2CH2CH(CH3)2. Show all reagents, and use curved arrows to show movement of electron pairs.