what is the inverse lever rule

I IUIAC-ION340DC564eecac03101af2döf56bb#10301 Home-AP Student. Elk Grove Unified - O My Profile - Zoom Results of the dhec.. VMy Citation list 9/2.. O Pearson Sign In 6 College Board -SAT. Reading list You may want to reference (Pages 258 - 262) section 6.4 while completing this problem. Constants Perodic Table Part A An unknown mass of each of the following substances, initially at 25.0 °C. absorbs 1960 J of heat. The final temperature is recorded as indicated. Find the mass of each substance. a. Pyrex glass (T = 55.6 C) Express your answer using two significant figures. m = Submit Previous Answers Request Answer X Incorrect; Try Again; 14 attempts remaining Part B sand (Ty = 62.3 C) P Pearson Copyright © 2021 Pearson Education Inc. All rights reserved. Terms of Use Privacy Policy Permissions | Contact Us | V I 2:42

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

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