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- Notice that the carboxylic acid is a jumping off point to get to other types of molecular connection, replacing the -H on the hydroxy part with another carbon group to get an________, replacing the -OH with a chlorine to get an________, replacing the -H on the hydroxyl again with a carbonyl related group to get an________, or replacing the OH with an amine to get an_________.Chemistry QuestionWhat is the missing reactant in this organic reaction? || CH3-C- CH2 -NH2 R No Answer A CH3 CH3-N-CH₂ || C−NH–CH2 C-CH3 + H₂O Specifically, in the drawing area below draw the structure of R. If there is more than one reasonable answer, you can draw any one of them. If there is no reasonable answer, check the No answer box under the drawing area. Note for advanced students: you may assume no products other than those shown above are formed. Click and drag to start drawing a structure. || X :0 Ś
- N H₂SO4 HO Click and drag to start drawing a structure.In the drawing area below, create an acetal with at least 3 methoxy groups, and a total of 5 carbon atoms.Your Question :help please answer in text form with proper workings and explanation for each and every part and steps with concept and introduction no AI no copy paste remember answer must be in proper format with all working!
- Ether groups are formed when alcohols are treated with acid. Consider the following question that focuses on acid-catalyzed ether formation using alcohol functional groups. There are 3 unique ether products will be formed when the following reaction is performed. Draw the product of the above reaction that has six carbon atoms and an ether functional group. **Be sure to include all lone pairs of electrons.**Good hand writing Explain every option... What product they makeFor the cation shown, four resonance structures are possible. Two resonance forms are given, but they are incomplete. Complete structures 1 and 2 by adding nonbonding electrons and formal charges. Complete the two remaining resonance structures according to their description, including nonbonding electrons and formal charges. Structure 1: add lone pairs and charges X H₂C H₂C CH3 CH₂ Structure 2: add lone pairs and charges H₂C H₂C 0- CH₂ CH₂
- Drag and drop the appropriate labels next to the indicated functional groups. LHOT HO, Amide Alcohol Ether Alkene 3° amine Ester Alkyne Ketone 2° amineUse the dropdown menus to choose the correct name for each structure shown. V [ Select ] H. 2-methylbenzoic acid CH3 ethylcyclocarboxylic acid 2-methylcyclocarboxylic acid 2-ethylbenzoic acid ( Select ) -C-OH O CH, -CH,-C [ Select] CH, | Select ) CH,-CH-CH2-c-o-CH, CH-CH-NH-CH, CH, | Select ) H3C CH3 'N | elect ] Use the dropdown menus to choose the correct name for each structure shown, ( Select ) H. CH3 COH V[ Select ) 2,2,2-trichloroethanoicacid 1,1,1 trichloro-2-carboxyethane 1, 2,2 chloroethanoic acid 2,2,2-chloroethanoic acid O CH, но---сн,-сн,--он [Select CH, ( Select ] CH-CH, -CH2-č-o-CH, CH,-CH-NH-CH, [ Select ] CH, H3C CH3 [ Select [ Select) H. CH3 [ Select) -c-OH CH, HO-E-C-CH,-CH, CH, OH [Select ) 2,2 dimethyl-1,5-pentanedioic acid 3,3-dimethylpentanedioic acid 2,2-dimethylpetanoic acid CH,-CH, -CH2-c-o-CH 2,2-dimethylpetanedioic acid CH,-CH-NH-CH, CH, ( Select] H3C CH3 'N' [ Select )A student suggests that the molecule on the right can be made from a single molecule with one less ring in it. If the student is correct, draw the starting material below, otherwise, check the box under the drawing area. ? + NaOH Click and drag to start drawing a structure. olo Ar