10) Please draw structures for the following names. (9 points) b) 2,5-dimethyl-5-sec-butyl decane c) 3-tert-butyl-3-ethyl cycloheptane

Q: (a) Draw the chair form of cis-1,4-dimethylcyclohexane. Show the strains present, and calculate the…

A: Since your question has multiple sub-parts, we will answer first three sub-parts for you. If you…

Q: Draw 4-ethyl-2,2,3,5-tetramethylnonane How many H atoms are bonded to carbon 2? Answer: and number…

A: Draw the structure and determine number of H atoms are bonded to Carbon-2 ?

Q: any conjugated portions in the molecules below: Answer A. CH3 CH2 Answer: B.

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Q: Answer the following parts (a-c) based on the Newman projection shown below. Draw the exact…

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Q: 1) Draw an energy diagram for the rotation about the bond depicted in red in the molecule shown…

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Q: draw a newman projection of b viewed from C-2 to C-3 according to first template, using newman…

A: Conformational analysis.

Q: Starting from the Newman projection below, rotate the back carbon to provide the structure in an…

A: Here, two bulky groups are -Et and -Cl.  Fully eclipsed : the dihedral angle is 0°. This is least…

Q: Circle or write in the correct answer in the bold/underlined multiple choice below: 1. Among the…

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Q: Rank the overall bond strain of the cyclic alcohol molecules enumerated below based on a decreasing…

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Q: Question: How many C-types do each of the following compounds have? Label them a, b,c ...    And…

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Q: Compare columns I and II, and write A if the value in column lis greater than in II B if the value…

A: Given: C4H8 C5H10

Q: -o-CH,CH, он

A: Select the longest chain of carbon i.e. principle carbon chain numbering  naming (prefix + word root…

Q: sawhorse projection of the following structure (1,2-dibromopropane) in a conformation in а. which…

A:

Q: 5. Explain why A is much more stable than B? B NH

A: To explain why compound (A) is more stable than the compound (B)

Q: CH3 F CH3 CH3

A:

Q: 3. (20) Cyclohexane may go through ring-flipping as shown below. 5 (a) Draw both of the possible…

A:

Q: Focus

A: Focus only on carbon 1 For carbon 1, which group has the highest priority? why What enantiomer is…

Q: 10) Convert each Newman projection to the equivalent line-angle formula, and assign the IUPAC name.

A: As per guidelines , if multiple questions present , first question is allowed to answer, please…

Q: Carbocation stability is important in reaction mechanisms involving alcohols. Based on the general…

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Q: Draw all three stereoisomers of the compound shown below. Label each structure vou draw according to…

A: Draw all three stereoisomers of the compound shown below. Label each structure you draw according to…

Q: Rank the molecules below from least stable to most stable

A: we have been asked the stability of given ring structure

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Q: Question 4 What stereochemical and/or molecular requirement needs to be satisfied for an E2…

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Q: (a) Using Newman projections, draw all staggered and eclipsed conformations that result from 60°…

A: Since you have asked multiple question, we will solve the first question for you. If you want any…

Q: molecular

A: Please find the file attached for explanation

Q: Draw the curved arrows and the resulting resonance structure of meta-nitrobenzoate that shows a…

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Q: The Ka of methanol is 5.01 * 10-16. Which side of the following reaction is favored, reactants or…

A: There is one way to determine the whether the reactants and products are favored in a equilibrium.…

Q: Use cyclohexane template to draw both chair comformers. Must show each group as axial or equatorial.…

A:

Q: For each of the three horizontal series below, rank each molecule from highest (1) to lowest (4)…

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Q: pent-3-ene nylhex-3-ene nylhex-3-ene

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Q: СО-Н НО* 0-

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Q: Given cyclohexane in a chair conformation, draw the most stable isomer and conformation of…

A: Most stable isomer and conformation of 1,3-dibromocyclohexane:

Q: (CH),CCI Choose

A: "Since you have asked multiple questions, we will solve the first question for you. If you want any…

Q: Draw the contributing structure that results from resonance indicated by the curved arrow(s). • You…

A: Resonating structures are also known as contributing structures. These structures are basically…

Q: 5. Assign E and Z configuration and write complete IUPAC names for the given compounds. Br. CI H a

A:

Q: down Lescagon (dashrwedn? 3. Provide the hexagon structure for -1,4-ditert-butylcyclohexane. Also…

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Q: Draw the 3d representation, wedge representation, and fisher projection of the enatiomers of…

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Q: + c. H2C-NH-CH2-CH3 H2C-CH2-CH2- -CH3 or Reason: H3C- -CH2 -CH3 CH H3C- d. ČH3 CH3 or Reason:

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Q: Use flat representation of rings, not chair in the drawing. Determine the most and least stable.…

A: Stereochemistry is a branch of chemistry that deals with the arrangement of atoms in the space…

Q: 2-35 Predict which compound in each pair has the higher boiling point. Explain your prediction. (a)…

A: Please find the attachment.

Q: (a) Draw all stereoisomers formed by monochlorination of the cis and trans isomers of…

A: (a) The stereoisomers of all the monochlorinated products of cis-1,2-dimethylcyclobutane are shown…

Q: (e) Chlorocyclohexane (f) cis-1,2-dichlorocyclopentane (g) trans-1,2-dichlorocyclopentane

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Q: Draw the contributing structure that results from resonance indicated by the curved arrow(s). H-O •…

A: The shifting of the electrons from one atom to another one within a molecule is electron…

Q: The alkyne carbon-carbon bond vibrate at a O higher, It is stronger O higher, It is weaker O lower,…

A: Strongest bond will have the higher stretching frequency than the weaker bond

Q: II. Answer as directed 1. Write the IUPAC name of the following a CH3-CH-O-CH2-CH3 CH3 b.…

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Q: Answer the following questlon for Cis- 1-chloro - 3 - nethylegclolexane cyclohexane AG yalve (…

A: The given compound cis-1-Chloro-3-methyl cyclohexane   The isomer with  both methyl and chlorine…

Q: Compound B: Η Η Η Η Η Η Η Η Η H—c- Η H=C=H Η Select Draw the skeletal structure of Compound B. Draw…

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Acid Base Titration

An acid-base titration is the method of quantitative analysis for determining the concentration of an acid and base by exactly neutralizing it with a standard solution of base or acid having known concentration.