please answer all parts , thank you :) **Exercise on Stereochemistry and Structural Drawing:****2a. Task:** Using skeletal structure, draw the molecule: (1R,3S)-3-ethoxycyclohexanol.**2b. Task:** Draw the enantiomer of the molecule in (2a) and give the IUPAC name.Instructions: For each part, focus on the proper stereochemistry indicated by the (R) and (S) configurations. Remember to clearly show the three-dimensional orientation of the groups attached to the chiral centers.

a.) We need to draw the skeletal structure and place the groups on chiral center such that we can…

Answered: 2a. Using skeletal structure, draw the…

2a. Using skeletal structure, draw the molecule: (1R,3S)-3-ethoxycyclohexanol 2b. Draw the enantiomer of the molecule in (2a) and give the IUPAC name.

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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AutoSave w | homework – Saved to my Mac OFF ... Home Insert Draw Design Layout References Mailings Review View O Tell me R Share O Comments Calibri (Bo. v 11 v A A E vE v E v E E Aa v AaBbCcDdEe AaBbCcD AaBbCcDdE AaBb AaBbCcDdEe Paste BIU V ab x, x A v I v A v No Spacing Normal Heading 1 Heading 2 Title Styles Pane Dictate Sensitivity Please answer the following questions fully and to the best of your ability 1) Please state how you would synthesize the following polymer below and show the mechanism behind the reaction. Note that this also means you need to tell me which molecule you are starting with as well as specifying all conditions required. он OH 2) Will either the polymer or the monomers you used to make it show peaks if IR spectroscopy analysis was done on them, and if so where? How about if UV-vis spectroscopy was performed instead? Page 1 of 1 93 words E English (United States) O Focus 白

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A coil with 193 turns has a magnetic flux of 37.3 nT-m² through each turn when the current is 1.90 mA. (a) What is the inductance of the coil? What are the (b) inductance and (c) flux through each turn when the current is increased to 3.53 mA? (d) What is the maximum emf & across the coil when the current through it is given by i = (2.72 mA)cos(wt), where w = 205 rad/s? (a) Number 3.788894737 Units mH (b) Number 3.788894737 Units mH (c) Number i 6.929947369 Units nWb (d) Number i 2.112687705 Units V
AutoSave We hw OFF ... Home Insert Draw Design Layout References Mailings Review View O Tell me R Share O Comments Calibri (Bo.. v 11 v A A E vE v E v E E Aa v AaBbCcDdEe AaBbCcD AaBbCcDdE AaBb AaBbCcDdEe BIU V ab A • I v A v Paste х, х E= == No Spacing Normal Heading 1 Heading 2 Title Styles Pane Dictate Sensitivity C13 NMR Peaks Aldehydes RCO)R Aldehydes and ketones Carbaxylic R(CO)X Carbaxylic acid derivatives Ntrile Nitrile RCN CC C-C Alkyne Akyne R-CC-R RCH20 RCH2-O R4C RAC R3CH R3CH RCH2X X= C-C, C-O, Br, CI, N RCH2X R2CH2 RECH2 RCH3 RCH3 TMS TMS 220 200 180 160 140 120 100 80 60 40 20 Typical chemical shifts in 13c-NMR 9) Why do the peaks of associated with aldehydes (both in H NMR and C NMR) appear so much further downfield than other peaks? C13 NMR Peaks E Page 5 of 5 E English (United States) O Focus 295 words 白

Learning AA prod03-cnow-owl.cengagenow.com Login Learning Learning × Online tea... y dr. marlow... ember L... with We 3. AS surroundi... M 2BrF3 (9) Br2 (g) + 3F2 (9) 4. AG° = AH°... M 5. AG: Pre... 1req 6. AG: Enthal... Using standard thermodynamic data at 298 K, calculate the free energy change when 2.14 moles of BrF3 (9) react at standard conditions. Substance AG (kJ/mol) 7. AG fro... 1req Question Question Question 8. Calculat... 1req AG° = 9. Calculat... 1req BrF3 (9) -229.4 Br2(g) 3.1 F2(9) 0.0 kj