Question 1 Please predict the products for each of the following reactions: A A В BCD ос NaNH 1.03 2. H₂O 1. n-BuLi 2. Mel 9 H2SO4, H₂O HgSO4 B 10 2 Pd or Pt (catalyst) Lindlar's Catalyst - D₂ (deuterium) n-BuLi 3 1. NaNH, 2, Eter Na, ND3 (deuterium) 1. (Sia)2BH 2. H₂O₂, NaOH 0 D

Question 1 Please predict the products for each of the following reactions: A A В BCD ос NaNH 1.03 2. H₂O 1. n-BuLi 2. Mel 9 H2SO4, H₂O HgSO4 B 10 2 Pd or Pt (catalyst) Lindlar's Catalyst - D₂ (deuterium) n-BuLi 3 1. NaNH, 2, Eter Na, ND3 (deuterium) 1. (Sia)2BH 2. H₂O₂, NaOH 0 D

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...

See similar textbooks

Similar questions

What is the spring constant(k), at extension 0.3cm, in the following figure? 4. on 1+ + 0.3 + 0.4 + + * 0.1 0.2 Extension (cm) O a. 1000 N/m Ob. 0.1 m/N 1000 N/cm O C. O d. 10 N/m + 2) Force (N)
Is this mechanism correct
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
Drowser Time Limit: 0:20:00 Time Left:0:15:19 Glenton Morris: Attempt 1 160 40 3.0 Page 1: 140 - 35 3.0 120 10 25 100 2.0 80 60 Z 10 Page 2: 05- 20 0 2. Time is 10 Timetsk 10 Page 3: Of all the graphs shown above, what plot type is correctly represented? O second order Page 4: O no plot shown is valid 4. 1st order 3rd order OL X (W) FON
AutoSave Off H 2. U Document1 - Word P Search retroget R File Home Insert Design Layout References Mailings Review View Help A Share P Comments O Find - E Replace Times New Roma v 12 - A A Aa v A AaBbCcDc AaBbCcDc AaBbC AaBbCcC AaB 1 Normal Paste BIU v ab x, x A ev A v A - I No Spac. Heading 1 Heading 2 Dictate Editor Reuse Title A Select Files Clipboard Font Paragraph Styles Editing Editor Reuse Files Voice Consider a reversible reaction in equilibrium, CO (g) + 3 H2 (g) = CH4 (g) + H20 (g). How the equilibrium of the reaction is disturbed by adding (i) CO, (ii) H2, (iii) CH4, (iv) and H2O2 in the reaction? 한 (Ctri)- Page 1 of 1 W English (Canada) D. Focus 100% 40 words 8:06 AM W 26°C Mostly sunny 4) a O 08/06/2021
There's the information to go off please show work and if more than onw problem is done label so I know
09:45 The major product/s that form/s during the nitration of benzenesulfonic acid is? choose the correct answer from provided option OA O2N. HOS OB. SO3H O2N Add a caption... > Status (Custom)
CHM 431A Lab 7- 2021SP Given Data page Time Temperatu (min) C1. Boiling temp of water re (°C) 25.4 Initial temperature of water 32.5 Temperature of boiling water 44.9 3. 56.9 C2. Temperature change (AT) 4. 71.3 Mass of beaker 5. 86.6 100.2 Mass of beaker and water 7. 100.6 C3. Mass of water 8. 100.6 100.6 1. 2) 6.
5,6,7
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

need percent of water in the hydrate sample for all 3 tries to make sure work is correct