Construct a three-step synthesis of 1-bromopropane from propane by dragging the appropriate formulas into the bins. Note that each bin willl hold only one item, and not all of the given reagents or structures will be used. Reactant Reagent 1 Step 1 Product Reagent 2 Step 2 Product Reagent 3 Final Product (1-bromopropane) (propane) Br2 Br2 (CH)3CO K HBr ROOR HBr NBS ROOR HaC Нас Нас, Нас Нас НаС. hv CH2 CH2 CH Нс CH-Br CH-Br CH Нас Нас, нC Нас НаС Br Br Br

CH3 || CH3 H₂O H2SO4 CH3CHCH2CH2C—ОCH₂CH₂CHCH3 a. Draw the structure of the tetrahedral intermediate INITIALLY-FORMED in the reaction shown. • • • You do not have to consider stereochemistry. Do not include counter-ions, e.g., Na+, I, in your answer. In cases where there is more than one answer, just draw one. √n [ ChemDoodle Ⓡ b. Draw the structures of the organic products of the acyl transfer reaction. • You do not have to consider stereochemistry. Draw the neutral form of the products; no charges. Draw one structure per sketcher. Add additional

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Construct a three‑step synthesis of 1,2‑epoxycyclopentane from bromocyclopentane by dragging the appropriate formulas into the bins. Note that each bin should hold only one item, and not all of the given reagents or structures will be used.             Reactant  −→−−−−reagent 1 →reagent 1 Step 1 product  −→−−−−reagent 2 →reagent 2 Step 2 product  −→−−−−reagent 3 →reagent 3 Final product

k Curved arrows are used to illustrate the flow of electrons. Use the reaction conditions provided and follow the curved arrows to predict the reactant and the product of this reaction or mechanistic step(s). Include all lone pairs and charges as appropriate. Ignore stereochemistry. Ignore inorganic byproduct products. Edit Product OH HBr Edit Starting Ether + H CH3 Br: CH3Br

HW 10# 1 I need help with the last part (Part 3)

Synthesize From 0= Br -0 (target product) (starting material)

Q5. Synthesis: Show how to prepare any two of the following compounds. The stockroom contains bromobenzene, cyclopentanol, and simple alcohols and bromides of four carbon or less as a solvent. 1-phenyl-2-propanone cyclopentylethanal 2-methyl-3-hexanone or CHO

Answer question 40 only!! The other questions are for reference only!!!!

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