This molecule will undergoa bimolecular nucleophilic substitution reaction with hydraxide ion. Drawthe major organic product of that reaction, including correct stereochemistry using wedges and dashes. NaOH
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- 28. What is the major organic product of the following reaction? HO CI 1. (CH₂)₂Culi 2. H₂O A) I B) II C) III D) IV i c III ноха IVPlastic photochromic sunglasses are based on the following reversible rearrangement of a dye inside the lenses that occurs when the lenses are exposed to sunlight. The original dye absorbs UV light but not visible light and is thus colorless, while the rearrangement product absorbs visible light and is thus darkened. (a) Show the mechanism of the rearrangement. (b) Why does the rearrangement product absorb at a longer wavelength (visible light) than the original dye (UV)?MacBook Air Page |3 6. Give the complete mechanism for the following reaction. MgBr 1. 2. H,0* od of sluuslom anie b Aom ua (co (ogami 1omim ai ao sldasog cobo 7. Show the complete mechanism for the formation of a hemiactetal, when 3-methyl-2-butanone reacts with ethanol under acidic conditions (H2SO4).
- Classify each of the following organic reactions. reaction Hör H₂O 1) Hg(OAc)₂, H₂O aveau Br OH OH type of reaction (check all that apply) Odihydroxylation addition hydrogenation Dhalogenation halohydrin formation. subtraction halogenation hydrogenation addition halohydrin formation inhalation Odihydroxylation addition hydrogenation oxyhydration halogenationCambridge International AS Level Chemistry ot boe slo plgmes s al snsdismonooli End-of-chapter questions 1 1-bromobutane will undergo reactions when heated, as shown by reactions A and B. ot dwab on s bl auoltse s boaub svsd 20 swoll gab ods-suai la yel snoso sdr ssiganm n2 monl gnivims noiteibar VU luad CH;CH,CH,CH,Br B CH;CH,CH,CH,OH CH;CH,CH=CH, 90u S1s 2O1D Isdh tuo gomia sli ni qu dgid tod a guch pecoue For reactions A and B give the reagents used in each case. b Reaction A was repeated using 1-iodobutane instead of 1-bromobutane. Explain any difference in the rate of reaction observed. p bas- od mon c What type of organic reaction is A? d Show the mechanism for reaction A. e Reaction A was repeated with 2-bromo-2-methylpropane instead of 1-bromobutane. i Name the organic compound formed. elle ii The mechanism of the reaction with 2-bromo-2-methylpropane differs from the mechanism of smitas nosd asd i anol reaction A. Describe how the mechanisms differ. f What type of reaction is…a online.butlercc.edu/courses/1479546/quizzes/2495663/take Question 3 What are possible products for the following reaction? HBr + enanti omer O None of the above Br Br 4. O A) and C)
- PPh3, DIAD CH20H (A) THF mitsunobu H2N sreaction NH2 excess AGOH () (Ci3H20 INS) me I N-me meAlcohols can undergo a lot of different reaction mechanims. If the alcohol group (OH) is attaached to an aromatic core, how will the chemistry change as compared to a typical alkyl alcohol? A) The OH group will become more polarised and more nucleophilic. B) The OH group will become more susceptible to oxidation C) The OH group will become more polarised and therefore basic D) The OH group will become more polarised and therefore acidic.Draw a structural formula for the major organic product of the reaction shown below. CuLi Consider E/Z stereochemistry of alkenes. • Do not show stereochemistry in other cases. • You do not have to explicitly draw H atoms. • Do not include organocopper or inorganic ion by-products in your answer. C P opy aste ChemDoodle
- What is the major substitution product to the following reaction? Но OCH,CH3 Chapter 9 Homew..pdf IMG_4217 (1)jpeg MG 4217jpeg INReagent 3 list; commas separate the choices benzylamine,cyclohexlbromide, cyclohexylamine NaBH3CN catalytic H+, h30, NaOH Reagent 4 list; CH3(Ch2)2MgBr, cyclohexylamine NaBH3CN catalytic H+, Na2 Cr2 O7 H2O H2SO4,cyclohexabromide reagent 5 list; cyclohexylamine NaBH3CN catalytic H+,CH3(Ch2)2MgBr, cyclohexabromide, benzylamineIndicate the directivity of the molecule below, and indicate if it is an 'activator' or a 'deactivator.! CH3 O ortho-, para- directing deactivator O meta- directing deactivator ortho-, para- directing activator meta- directing activator 00