Say an alkene reacted with a peroxyacid like mCPBA, then hydrated after. Take note of the product at this point. Other than the procedure mentioned, what other reaction for alkenes will allow you to do the same thing? A Hydration with water B Hydroxylation with KMN04 in base c) Oxidative cleavage with ozone D Hydroboration-oxidation
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- 1) Complete the following reaction scheme. Show stereochemistry where necessary. Show all organic products. NBS UV 2) (a)Complete the following reaction scheme. Show stereochemistry where necessary b) Indicate the reaction type, SN1, SN2, E1 or E2 (c) Provide two reasons for the reaction type stated in (b) Reacton Pd Penon 2 Reacten Produd Feson2 Reaction Podet Reson 2 Peaction Product Reason 2 Tre OH Peacton Preduct aton Reason1 Reason2 HBr OH 3) For each of the following planar (flat) structures, indicate whether the structure is aromatic or non-aromatic он(4) Starting from a single carbon, showing all Hhe balance reactions and electron trans fer by arrows, synthesiged O Nephtkalone O Anthracene HOUOV TYNYASprovide the major profucts ( wrote "no reaxtion "if you think so) for the following reactions with correct stereochemistry. Please explain step by step with explanation
- [Review Topics] [References] Use the References to access important values if needed for this question. Draw the structural formula of the product that would form when 3-isopropylcyclopentene undergoes catalytic hydrogenation. • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. C P. opy aste ChemDoodle Submit Answer Retry Entire Group 4 more group attempts remaining Previousences] Use the References to access important values if needed for this question. Draw the organic product that is expected to form when the following compound is oxidized under biological conditions. oxidation CH,CH,SH reduction • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. • If no reaction occurs, draw the organic starting material. C. opy aate Pre ChemDoodle"Rank the reactivity of the following alkenes toward acid-catalyzed hydration from most reactive to least reactive. (The alkenes are not in the corect order).
- b) The following compound Z as shown in Diagram 3 is one of the minor products obtain fromthe termination steps in the mechanism of the reaction between alkane compound andchlorine gas in the presence of UV light. Based on the following compound, propose thecomplete propagation steps in the mechanism.4.) Use retrosynthetic analysis to show how hex-3-yne can be prepared from acetylene and any other organic and inorganic compounds. Then draw the synthesis in the synthetic direction, showing all needed reagents. mopeatane to athy alkene tat occus via a syn ion and drevs on occurs vi an anti addition d dras ia stte wote out two resctions on that Markov addition and notha tht kov parloway 5.) Devise a synthesis of CH3CH2CH2CHO from two-carbon starting materials. Draw both the retrosynthesis and the forward synthesis.[Review Topics] [References] Use the References to access important values if needed for this question. Draw the structure of the product that is expected when the following compound is treated with concentrated H2SO4. H2S04 CH,CH2CH,CH2CH2OH heat • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. C P. opy aste C. CH4 ChemDoodle Submit Answer Retry Entire Group 5 more group attempts remaining
- The following compound Z as shown in Diagram 3 is one of the minor products obtain fromthe termination steps in the mechanism of the reaction between alkane compound andchlorine gas in the presence of UV light. Based on the following compound, propose thecomplete propagation steps in the mechanism.Consider the molecule 3-hexyne, shown helow tf vou partially hydrogenated the molecule (1.e. generated nn alkene, rather than an alkane) and then treated the tina alken clemental bromine, illustrate the results if you hydrogenated over the Lindlar catalyst compared to hydrogenation via lithium or sodium in ammonia. CHgCH2C=CCH2CH3 Alkynes can be directly reacted with elemental bromine as well. Assuming that you could control this process to limit it to a single addition (i.e. generate an alkene), what would happen if you reacted first with bromine and then hydrogenated the result? Explain in the context of your answer above.Why does catalytic hydrogenation of alkenes proceed through syn addition? Provide a detailed explanation and illustrate as needed (5 sentences only).