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- Complete thoroughly and with lots of detailDraw a full Lewis structure for each following compound. Include lone pairs andnon-zero formal charges as necessary.a. HCN, hydrogen cyanideb. Si(OH)4, orthosilicic acid c. and d. are in photo attached. Look at cyclobutan-2,2-diol from d. Write the hybridizaOon of eitheroxygen atom (sp, sp2, or sp3). In Si(OH)4 (from question b.), write the hybridization of the silicon atom. Write compound in in this previous question that should exhibit a strong, sharp peak at 1712cm–1 in its IR spectrum.please answer them
- Please don't provide handwritten solution ....For anion NO2-, (a) predict the stereochemistry. Justify your prediction with VSEPR theory and by formal charge; (b) indicate the hybridization appropriate to the stereochemistry; (c) describe the bond character of N-O for the resonance structure.om/ilm/takeAssignment/takeCovalentActivity.do?locator-assignment-take eq [References] Identify the functional groups in the following molecules. (Use names from the table below. List each class of functional group only once. If there are fewer than 3 functional groups, leave an appropriate number of answer boxes empty.) a) OH b) CH3 Name 2req Alkene 2req Structures of Some Common Functional Groups Structure Nitro Name Structure SH 2req Alkyne -C=C Thiol 2req Arene Aldehyde pts 2req 4 3 Halide Ketone (X = F, Cl, Br, I) OH Alcohol Carboxylic Acid A F4 DII Cengage Learning Cengage Technical Support * PrtScn Home FB F9 & 85 % 6 7 29 E R T Y U End F10 PgUp ( ) 8 9 0 - ク F GH J KLMm.31. Subject :- Chemistrya) Predict the major product of the reaction and identify the type of reaction (substitution or addition). Explain the function of Pt used in the reaction. (with First image) b) Write the reaction of the mononitration of chlorobenzene and predict the major products with reasons. c) Identify all the carbon atoms in the following compounds that are sp2 (Circle the carbon(s) your selected on image two)In aqueous solution, a molecule of glyceraldehyde (shown below) can... OH OH I H-C-C-C II H H O= H donate up to 2 H-bonds and accept up to 6 H-bonds. donate up to 6 H-bonds and accept up to 2 H-bonds. H-bonds and accept up to 3 H-bonds. donate up to 2 donate up to 3 H-bonds and accept up to 6 H-bonds. donate up to 5 H-bonds and accept up to 3 H-bonds.I got the answer wrong. I am having trouble distinguishing between molecules that have and dont have delocalized electrons. Can someone verify , do positive charges, conjugation mean the molecule is delocalized? thanks for any explanationCan you please explain to me how I can better identify the IMF in organic chemistry? I have trouble looking at the molecules and being able to tell what forces are at play.4. Outline the following synthesis (a). Butane to 2-butanol (b). 1,2-dibromopropane from 2-propanol (c). 1-butanol to 2-butanol (d). Propane to PropeneSEE MORE QUESTIONS

