Be sure to answer all parts.Identify the lettered compounds in the following reactions. Draw your structures as three-dimerepresentations using chair pyranose rings. Include ALL hydrogen atoms on the pyranose ring!draw the bonds to the methyl groups.OHHOCH3IH3O+DHOOHAg₂OE + F + CH3OHOH(Both anomers of E and F are formed.)HO0HOOHOHH# #edit structure ...Ꭰedit structure ...finish structure ...EF

Step 1:Step 2:Step 3: Here, in step 1: the free -OH groups are converted into ethers in presence of…

Answered: Be sure to answer all parts. Identify…

Chemistry

10th Edition

ISBN:9781305957404

Author:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Publisher:Steven S. Zumdahl, Susan A. Zumdahl, Donald J. DeCoste

Chapter1: Chemical Foundations

Section: Chapter Questions

Problem 1RQ: Define and explain the differences between the following terms. a. law and theory b. theory and...

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Predict the major products of the following organic reaction: Δ + ? NC Some important Notes: Draw the major product, or products, of the reaction in the drawing area below. If there aren't any products, because no reaction will take place, check the box below the drawing area instead. Be sure to draw bonds carefully to show important geometric relationships between substituents. Click and drag to start drawing a structure.
What reagent is necessary to complete the reaction? CH3-CH2-CH-C-OH ? CHỊCH,CH C-0- Na* CH3 CH3 NaO O NaCl O Na O NaOH + H₂O
Name the following compounds and show how you numbered each carbon atom. note: I need the answer immediately. I will send a good rate right away as well.
CH=CHCN 3-phenylpropenenitrile Electrophilic substitution on 3-phenylpropenenitrile occurs at the meta position. Draw resonance structures to show how the ring is electron-poor at the ortho and para positions. ● • You do not have to consider stereochemistry. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate resonance structures using the → symbol from the drop-down menu.
Draw an arrow-pushing mechanism to show the first step in the hydration of acetone under basic conditions. Use only the reagents shown. Represent KOH as "OH. Show all nonzero formal charges and lone pairs of electrons. HÖ: :ÖH Кон H20 H.C CH H,C CH, Draw the missing reagent and the missing curved arrow notation.
OH OH 01C O 01C + CH3-C-0-C-CH3 Imidasool
Draw a structural formula for the missing organic product in the reaction below. + CH;CH,NHCH2CH3 CH3CH2CH2CH2CH,COCCH,CH2CH,CH,CH3 CH;CH,CH,CH,CH2COH
Which of the following is an anti addition? O Addition of C12 and H2O across an alkene Addition of H2 across an alkene O Dihydroxylation of an alkene using OsO4 o Formation of an epoxide from an alkene using mCPBA
Draw a structural formula for 2,2-dimethylpropanoic acid. O • You do not have to consider stereochemistry. • You do not have to explicitly draw H atoms. 9-85 +▾ / / CH4 o Jn [t ChemDoodle ?
Draw the major product that forms for the following reaction. Use a line structure which means that you should not draw in H atoms and should not enter C for carbons unless necessary. Convert your answer to the InChl format and enter it as your answer. Not all possible products may be provided as a response. CH3 AICI, < 5 C H3C CI
H 1) 2-ethyl-2-methyl-1,3-dioxolane pTsOH 2)LIAIH4 Me 3)HCI Me (60%) 36a myrtine
CH,CH3 Br ČH3 If you take the above compound, and place an ISOPROPYL group on the carbon of the ring directly between the bromo and methyl groups, you will have a ring with four groups, all on different neighboring carbons. The correct IUPAC name of this new compound would be (including numbers and proper punctuation when required): toluene

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