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- (UV spectroscopy lab, organic chem 2) Perhaps it is unsurprising that cyclohexane and ethanol are reasonable UV solvents, whereas toluene is not. Explain why that is. please answer, in detail- will give a thumbs up. thank youProvide the missing reagent to complete the following reaction. CH,CH,CH,ÔNa ? Write your answer on separate paper and submit a picture of your work here. Attach File Browse Local Files A Moving to another question will save this response.What reagents, also including solvents and or temperature needed, would go above and below the arrows and then what would the final products be?
- Please answer this NEATLY, COMPLETELY, and CORRECTLY for an UPVOTE. Supply the reagent for the reaction shown below.2. What reaction conditions would you use to carry out the following conversions. Note include all steps of the reaction including work up as necessary.For each of the following, write the major product(s) and then draw out each step in the mechanism using curved arrows. Show ALL lone pair electrons and formal charges. Redraw ALL molecules as to show explicitly ALL bonds being broken or formed. Identify the molecular orbital (HOMO) of the nucleophile and the molecular orbital (LUMO) of electrophile involved in the nucleophilic attack. MO diagrams are not necessary..
- Please do it... It is a single question perform retrosynthetic analysis on the given molecule. Your starting materials should be limited to unfunctionalized alkanes (except as noted). use reaction such as SN1, SN2, E1, and E2Be sure to answer all parts. For the following alkyl bromide, draw the major and minor products that result from dehydrohalogenation. Br "OH The major product is: draw structure .. The minor product is: draw siructureAcyl transfer (nucleophilic substitution at carbonyl) reactions proceed in two stages via a "tetrahedral intermediate." Draw the tetrahedral intermediate as it is first formed in the following reaction. H3C HCI / H2O `NH2 reflux • You do not have to consider stereochemistry. • Include all valence lone pairs in your answer. • Do not include counter-ions, e.g., Na", I, in your answer. • In cases where there is more than one answer, just draw one. opy aste Previous Next
- Complete the following for the below reaction. i. draw the complete Molecular Orbital diagram with electron filling, nodes and phasing. ii. label each level with the number of bonding and antibonding interactions iii. label each level as bonding, nonbonding or antibonding, and HOMO & LUMO iv. Using the correct level, show how the cyclization occurs to give cyclohexadiene and indicate whether the product is cis or trans. heatWhat's an appropriate reagents/conditions that goes inside the box (step 2)please do all syntheses and also show disconnections and synthons..