Expierement #9 5a7c3f5a5de34531825e9ce379aaaabe

Choose reagents to convert 2-cyclohexenone to the following compounds. Syntheses may require several steps. Use letters from the table to list reagents in the order used (first at the left). i 1. Li(CH2=CH)2Cu Reagents a 1. Li(CH3)2Cu 2. H3O+ e 1. Li(C6H5)2Cu 2. H3O+ b 1. NaBH4 f CH2l2/Zn(Cu) / ether j 2. H3O+ C NH3 / KOH g 1. CH3MgBr/dry ether k 2 H3O+ d H2NNH2/KOH h HN(CH3)2 HO CH3 a) b) OH N(CH3)2 2. H3O+ (C6H5)3P+-CH2 H₂ over Pd/C KMnO4/H3O+

CH3 H CH3 CH3 When isopropylidenecyclohexane is treated with strong acid at room temperature, isomerization occurs in two steps to yield 1-isopropylcyclohexene. One of these steps is shown below, add curved arrows to the mechanism to indicate the movement of electrons in this step. Arrow-pushing Instructions -XT H-CI CH3 H* CH3 CH3 CH3 -H CH3 CI

Choose reagents to convert 2-cyclohexenone to the following compounds.

Choose the reagents that can be used to achieve the following conversion. More than one reaction is required, and reactions from earlier chapters may be necessary. Reagents may be used more than once. CH3-CH2-C-CH3 CH3-CH=CH-CH3 H2SO4 H,SO, 1 2. 180°C 140°C (0) H2 3. 4 Pt H+ H20 5. 6. CH;OH H2SO, (Enter multiple answers as a comma-separated list.)

Draw the major product from this reaction. Use a dash and/or wedge bond to indicate the stereochemistry of substituents on asymmetric centers, where applicable. Ignore acid byproduct. + Q 1. Br2, H₂O 2. NaOH Drawing Q

Draw the alkene that would react with the reagent given to account for the product formed. CH3 H2S04 ? H2O CH3CCH3 HO. • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. In cases where there is more than one answer, just draw one.

The theoretical yield of 1-methylcyclohexene in moles(from 2-methylcyclohexanol amount of 2.239 gram).  The theoretical yield of 1-methylcyclohexene in moles is 0.01961. 1. What is the corrected actual yield(% Relative Area for 1-methylcyclohexene is 82.81%)? The theoretical yield of 1-methylcyclohexene in moles is 0.01961. 2. . What is the calculation of the %yield of 1-methylcyclohexene?

Do

H₂SO4 CH3 CH3CH₂C=CH₂ CH3OH CH3CH₂ -OCH3 CH3 Treating 2-methyl-1-butene with methanol in the presence of sulfuric acid gives 2- methoxy-2-methylbutane. Draw curved arrows to show the movement of electrons in this step of the reaction mechanism. Arrow-pushing Instructions H + H-O-CH3 H-O-CH3 AOC XT CH3 CH3 H₂ H3C-C-C=CH₂

Use the References to access important values if needed for this question. Which reagent would be expected to bring about the following conversion? CH3 CH3 CH,CHCHCH3 CH=CHCHCH3 ÓH O 02 O HCI O H2 O H20 O Cl2

II. Apply all the criteria for each reaction, and then draw the product(s) of each. a) b) 9 d) Br X² CH3CH₂O CH3 Br CH3 CH3 Br + j EtOH CH3CH₂CI CH3OH heat ? CH3ONa CH3OH ? ? i ? 1

From the table of available reagents select the one(s) you would use to convert:3-pentanol to 3-bromopentane:cyclopentanol to trans-2-methylcyclopentanol:Use the minimum number of steps; in no case are more than four steps necessary.List reagents by letter in the order that they are used; example: fa.

Draw the major product(s) of the following reactions including stereochemistry when it is appropriate. CH;CH2-C=C-CH3 1 C2 • Consider E/ Z stereochemistry of alkenes. If there is more than one major product possible, draw all of them. Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner.

It’s wrong please help

Draw a structural formula for the major organic product of the reaction shown below. ether CH-CH-CH-CH=C CH2CH3 H₂O + (CH3)2CuLi Cl You do not have to consider stereochemistry. 0 / 46 94 LIF ChemDoodle

6n) For the E2 reaction of deuterated 1-bromo-2-methylcyclohexane, which of the following three molecules is the correct product? (Note: D is the atomic symbol for deuterium, an isotope of hydrogen.) DH H CH₁₂ -OCH₁ Br H CH3 H CH3 ؟؟ D b) DH a) HO H CH H

Draw the product of the reaction shown < below. Use a dash or wedge bond to indicate the stereochemistry of substituents on asymmetric centers. Ignore inorganic byproducts. 1. NaBH4 2. H3O+

me following multistep synthesis of the target structure on right from the starting structure on the left choose the correct order of reagents. Ignore stereochemistry. To preview the image click here & Step 1 Step 2 Step 3 Br. 요 Step 4 Step 5 Step 1 Reagent(s) [Select] Step 2 Reagent(s) [Select] Step 3 Reagent(s) [Select] Step 4 Reagent(s) [Select] Step 5 Reagent(s) [Select]

1,5-methano[10]annulene is stable at room temperature, but [10]annulene is not stable at room temperature.Why is there a difference in reactivity?

Yead. III. Show a complete synthesis of the following molecule starting with cyclohexane (as many times as you wish), any molecules of three (3) carbons or fewer, and any other reagents. (16 pts) Zoxo 5 Br BV-Br +Br HBV Br-Br Br Br Br Br Br HBV Br Br Brz ← ·Br Br BL Δ H G HO) TH F -OH он して

Fill in the missing reagents in the boxes below. some steps may require more than one step.

What is the IUPAC name for this molecule?

CrO3 CH3CH2CH2OH CH3CH2COH CH3CH2COCH2CH2CH3 A problem often encountered in the oxidation of primary alcohols is that esters are sometimes produced as by-products. For example, oxidation of propyl alcohol yields propanoic acid and propyl propanoate. Draw curved arrows to show the movement of electrons in this step of the reaction mechanism. Arrow-pushing Instructions B: :0: CH3CH2CH- A: BH* CH;CH,CH нӧ: HÖ H-A