Q: 3. Write formulas to show the possible geometric isomers of dibenzalacetone. Which isomer would you…
A: Geometrical isomers are also called as cis/trans isomers. In cis isomer the same groups or atoms…
Q: Could you put them each in order from "Most electrophilic to the Least electrophillic? Thanks
A: Electron donation or acceptance is also possible by resonance
Q: 1) Consider the acid-base reaction below. A) Predict the products and show the arrow-pushing…
A: The reaction between propanoic acid and sodium ethoxide gives sodium propionate and ethanol. The…
Q: The decalinols A and B can be equilibrated using aluminum isopropoxide in 2-propanol (isopropyl…
A:
Q: R [0] H Specifically, in the drawing area below draw the skeletal ("line") structure of R. If there…
A: In the given reaction, on the product side there is an aldehyde. The reactant get oxidized and…
Q: Step 1: When a curved arrow starts from a o bond and points to an atom, the o bond breaks. If the…
A: The reactant that is undergoing splitting is C6H5 - CH2 - Br Here the C - Br bond of CH2 - Br is…
Q: Include all lone pairs and charges as appropriate. Use wedge and dash bonds to indicate…
A: Mechanism: When a departing group leaves, a nucleophile hits the substrate simultaneously. As a…
Q: Styrofoam dissolves in gasoline (gas), why? OA) Both are polar and they mix OB) Both are non-polar…
A:
Q: 1. Use your knowledge of the M0 diagrams for the species shown below to describe each orbital in…
A: The combination of two or more number of elements in different proportions produces the compounds.…
Q: Use the References to access important values if needed for this question. Complete the equation for…
A: The question explains the reaction between secondary amine and carboxylic acid to form corresponding…
Q: Can the molecule on the right-hand side of this organic reaction be made in good yield from no more…
A:
Q: 4. Draw two resonance structures better than the structure provided. Draw curvy arrows to show how…
A: To draw two resonance structures better than the structure provided. Draw curvy arrows to show how…
Q: Copy the figure shown below onto your scratch paper. Вох 1 Воx 2 HBr H2NCH3 NHCH, Br Then, complete…
A: A nucleophile attacks on a alpha-carbon atom of a compound and substitute a leaving group via SN2 or…
Q: Draw the structure(s) of the major organic product(s) of the following reaction. CrO3 / H3O+ • You…
A: CrO3/H3O+ is Jones reagent, an oxidising agent that oxidises primary alcohol to aldehyde and…
Q: Is the group of atoms indicated with an arrow nucleophilic, electrophilic, acidic, more than one of…
A: Phenol, also known as carbolic acid, is an aromatic organic compound with the chemical formula…
Q: Draw structural formulas for the major organic product(s) of the reaction shown below.
A: The reaction of chlorobenzene with nitric acid in the presence of concentrated sulphuric acid is as…
Q: 2. Mechanisms and molecular structure: a) The following reaction can happen in cells with the help…
A: The objective of the question is to understand the molecular structure and mechanisms of a reaction…
Q: Complete this sentence based on what you’ve learned above: If CO2 levels increase, the reaction will…
A: The balance chemical equation for a reaction between CO2 and H2O is as follow CO2 +…
Q: Draw both resonance structures of the most stable carbocation intermediate in the reaction shown. +…
A: Benzyl > Allyl > Tertiary > Secondary > Primary > Methyl
Q: the isommeric fonship between tne mo Your choices are dieastereomers, enantiomers, identical, or…
A: Isomers are compounds which have same chemical formula or numbers of atoms but differ in structures…
Q: Decide which compound in each of the following pairs is more stable. (Please explain)
A: The pairs given are,
Q: Draw both resonance structures of the most stable carbocation intermediate in the reaction shown. +…
A: Product of following reaction can be made by applying appropriate reaction mechanism.
Q: Draw the structure(s) of the major organic product(s) of the following reaction. HCI + но- You do…
A: In presence of diol, and non aqueous acid, carbonyl compound undergo acetal-ketal reaction to form…
Q: Copy the figure shown below onto your scratch paper. Box 1 Вох 2 Box 3 HBr Br Then, complete the…
A:
Q: A is an aromatic compound with the molecular formula C,HeN. Draw the structure of A. C,H;N (an…
A: This question can be solved using the Double bond equivalent concept, DBE=122n4+n3-n1+2 Where, n4 is…
Q: 1) Please use line-angle notation to illustrate the acid base reaction which would occur between the…
A:
Q: Fill in the lable below with as appropriate to rank tne expected nydrophilicity eac illustrated…
A:
Q: Below you will find twelve (12) structures (e.g. structure 1, structure 2, etc....some represent…
A: a) The product formed in this reaction is given below: The reaction proceeds via a three-step…
Q: 2. Alcohol Substitution - Predict the product(s) OR starting material of the following reactions.…
A:
Q: 47. Dimethyl amine, (CH);NH, is a weaker base than NH3 48. Neutral iron (III) chloride is uscd to…
A: An organic compound that consists of two methyl groups and an amine group. It is also called a…
Q: OCH3 ОСН3 + Br2 FeBr3 D
A: Given is organic reaction.Given reaction is aromatic electrophilic substitution reaction.The name of…
Q: Between the following radicals; which one is more stable? I or II PHHC(*)CH2ET (1) PHCH2C(*)HEt (1I)…
A: Given free radicals are PhHC(•)CH2Et (I) PhCH2C(•)HEt (II) The free radical with more…
Q: Draw structural formulas for the major organic product(s) of the reaction CN S AICI3 + (CH3)2CHCI .…
A: A chemical reactionMajor organic product(s) of reaction: Need to be determine
Q: and label all of the functional groups that you see (identified in the table above). Please note the…
A: Functional group is a substituent in a molecule consisting of group of atoms that changes the…
Q: Predict the products of this organic reaction: + H₂O + HCI ? Specifically, in the drawing area below…
A: In presence of any acid (HCl) and h2o water ,amine hydrolysis takes place to form carboxylic acid…
Q: aw a structural formula for the major product of the acid-base reaction shown. NH₂ (1 mole) • You do…
A: Product of following reaction can be made by applying appropriate reaction mechanism.
Q: I need solution with explanation. Please don't provide handwritten soluion.
A: The objective of the question is to determine the position(s) where an electrophilic substitution…
Q: Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product…
A: Given data:Draw curved arrow.Grignard reagent is the source of the nucleophile. It is mainly used…
Q: Although it seems as if free radical chemistry is of essential but limited use in organic chemistry,…
A:
Q: Subject: organic Chemistry Instruction: Classify each reaction as oxidation, reduction, or neither.…
A: NOTE: Since you've posted multiple sub-parts, we'll solve only the first three sub-parts for you. To…
Q: There maybe more than one correct answer for the following question, select all that apply. The…
A: The entropy of the system is the measure of the degree of randomness or the disorderliness in the…
Q: Use the References to access important values if needed for this question. Complete the equation for…
A: We have been given one incomplete reaction.We have been missing organic product in one organic…
Q: (Chapter 9) Write all of the resonance contributors for the following molecule. If the various…
A: The resonance structure of a compound is formed when the lone pair of electrons present on an atom…
Q: Choose the two words which complete the following sentence to make a true statement. As the number…
A:
Q: II) Reactions - Complete the following reactions by drawing clear structures for the major organic…
A: Given are organic reactions. Note: According to our guidelines we are supposed to answer only first…
Q: 3) Review the three structures provided below. (Hint: Convert to extended formula or Lewis Dot…
A: More basic the base more will be the pKa of it and hence it will abstract protons easily.
In A negative charge on oxygen atom.
In B negative charge on the carbon atom.
Step by step
Solved in 3 steps
- a) Draw the ring-flip isomer of the molecule from question (b) Show which of the two is favored in the equilibrium between them, and explain why, showing all possible forms of strain in each of the isomers. (c) What is the stereochemical relationship between the two isomers? (d) Draw another stereoisomer of the molecule and show all the strains it contains.(strains is the most important one in this questuon!!!)The structure shown below is has a very high pKa because the conjugate base is very unstable. Using the provided resonance structures, draw the curved electron-pushing arrows to show the deprotonation step. Then, draw the curved electron-pushing arrows to show the interconversion between resonance hybrid contributors. Be sure to account for all bond-breaking and bond-making steps. H Select to Add Arrows CH3CH2CH2CH2Li H Select to Edit Arrows H H LIⒸOn the molecules on the back page, circle and label all of the functional groups that you see (identified in the table above). Please note the following tips that may help you on this assignment: If a molecule contains –COOH, or a C double bonded to an O and single-bonded to an –OH, the functional group you circle is only the carboxyl, not a carboxyl, carbonyl, and hydroxyl separately). Phosphate groups are tricky – any P surrounded by 4 O’s is a phosphate – adjacent phosphates may share an O, and sometimes the O is in the form of OH. There is often shorthand that is used in drawing these structures – if you see a jagged line or ring structure, assume that carbon is at each corner. There may be ionized forms of the functional groups above (such as NH2 or NH3+) – these are the same functional groups. The order of the atoms in the functional group may be switched, depending on which side of the molecule it is on. For example, “—NH3” and “H3N—“ are the same thing.
- A=B When a curved arrow starts from an bond and points to an adjacent atom, the n bond breaks and the o bond remains. This will typically generate two charges. A-B=C Note in the second mechanism shown, if the first curved arrow started from atom C, then atom B would violate the octet rule. A second a bond would need to delocalize. Read the curved arrow in the mechanism shown and draw the product. Be sure to draw lone pairs. Select Draw Rings More Erase C HPlease answer all part of the question...thank you[References] Draw structures for the alkene (or alkenes) that gives the following reaction product. Br CH3CH₂CHCCHCH3 II Br CH3 Br₂ • You do not have to consider stereochemistry. • Submit more than one structure only if the structures are constitutional isomers. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the ● Separate structures with + signs from the drop-down menu. e- ChemDoodle {}
- answer with explanation please!!Need help solving this, please show your work with the answer!On the molecules on the back page, circle and label all of the functional groups that you see (identified in the table above). Please note the following tips that may help you on this assignment: If a molecule contains –COOH, or a C double bonded to an O and single-bonded to an –OH, the functional group you circle is only the carboxyl, not a carboxyl, carbonyl, and hydroxyl separately). Phosphate groups are tricky – any P surrounded by 4 O’s is a phosphate – adjacent phosphates may share an O, and sometimes the O is in the form of OH. There is often shorthand that is used in drawing these structures – if you see a jagged line or ring structure, assume that carbon is at each corner. There may be ionized forms of the functional groups above (such as NH2 or NH3+) – these are the same functional groups. The order of the atoms in the functional group may be switched, depending on which side of the molecule it is on. For example, “—NH3” and “H3N—“ are the same thing.
- Four isomers A-D with the formula C5H12O exhibit different reactivity patterns as indicated below. Isomer A reacts with PCC and CrO3 to provide identical products. Isomer B reacts with PCC and CrO3 to provide different products. Isomers C and D do not react with either PCC or CrO3. Isomers A, B, and C readily react with NaH but D does not show any reactivity with NaH. The 1H NMR splitting patterns for these isomers are as follows. Isomer A: δ 0.91 (d, 3H), 0.90 (d, 3H), 1.18 (d, 3H), 1.92 (dqq, 1H), 3.38 (dq, 1H), 3.58 (bs, 1H). Isomer B: δ 1.25 (s, 9H), 3.45 (s, 2H), 3.65 (bs, 1H). Isomer C: δ 0.90 (t, 3H), 1.44 (q, 2H), 1.24 (s, 6H), 3.65 (bs, 1H). Isomer D: δ 1.10 (t, 3H), 1.13 (d, 6H), 3.19 (septet, 1H), 3.50 (q, 2H). Based on all of this information, provide the structures of A-D. (Note: If there is a chiral center on any of these molecules, assume the stereochemistry as “R”. dqq=doublet of a quartet of a quartet, bs=broad singlet)Please don't provide handwritten solution.....Draw both resonance structures of the anion formed by the reaction of the most acidic C-H bond of the compound below with base. • Include all valence lone pairs in your answer. . For structures having different hydrogens of comparable acidity, assume that the reaction occurs at the less-substituted carbon. • Draw one structure per sketcher. Add additional sketchers using the drop-down menu in the bottom right corner. Separate resonance structures using the symbol from the drop-down menu. 0- O Bi % 5 T G ▾ 99-85 A 6 SCH₂CH3 ChemDoodleⓇ Cengage Learning Cengage Technical Support Y H F6 On [F & 7 O U J F7 * 8 PrtScn | K Home 9 83°F Sunny O L A End 0 F10 P IN Previous Next> C 4x PgUp F11 J Save and Exit 9:38 AM 7/18/2022 PgDn + = F12 80