Is the following a diasteromer, constitutional, enantimoer, or the same compound?

Q: Which TWO of the bromides shown would undergo hydrolysis to provide the same carbocation…

A: In the hydrolysis reaction, carbocation formed removing halide ion. Carbocation can rearrange to get…

Q: Chair conformation of glucose, galactose , and fructose

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Q: Draw all configurational isomers of C4H11N that are optically active.

A: Optically active compounds are those which rotates the plane of polarised light.

Q: Match the images with the correct conformation term. CH3 CH3 H,C. H,c CH, Answer Bank anti eclipsed…

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Q: Please draw the structures of all dimethylcyclobutanes and circle those that are chiral.

A: An asymmetric carbon atom( Chiral carbon) is a carbon atom that is attached to four different types…

Q: Determine absolute configurations for the double bond and chiral carbon for the molecule shown. OH…

A: RS nomenclature: The RS nomenclature is an important nomenclature system for denoting the…

Q: Show stereochemistry only if given in the name. • In cases where there is more than one answer, just…

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Q: Is there no stereochemistry for any of these molecules?

A: Sterio isomers are compounds having  same molecular formula and same structure but different…

Q: 7.79 We treat each chiral center separately. For each chiral center, we redraw one of the horizontal…

A: We give priority according to CIP rule. In this rule the group with highest atomic number is given…

Q: CH3 CH3 11 |13 12 2 10 8, 14 3 4 6 7 a) Substituent Up at C4. b) Substituent Up at C11| c)…

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Q: How would the conformation look if a ring flip occured

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Q: Question attached

A: The chiral carbon or chiral center is the carbon or any atom which has all different substituents…

Q: (A) (В) (С) (D)

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Q: For the following chair conformations of 1,4-dibromocyclohexane, determine the orientations of the…

A: Conformation  Shape adopted by a molecule caused by the rotation around one or more single bonds.

Q: State the Newman projections for the staggered and eclipsed conformations of propane ?

A: Newman projection is represented with front atom as dot and back atom with circle. It has two…

Q: Which of the following is the most stable conformation of the following con 111 IV IN MI

A: The objective of this question is to show the most stable conformation of given molecules Given is…

Q: Which of the following correctly lists the conformations of cyclohexane in order of increasing…

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Q: Draw the following structure in the most stable chair form. Justify.

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Q: OH

A: Stereoisomers are those isomers that have same molecular formula but different three dimensional…

Q: 22 Which is the least stable conformation of cyclohexane? a) boat b) chair c) envelope d) allsix…

A: Ring flipping is another process that cyclohexane can go through to switch between the boat and…

Q: CH, CH, Br CI CH,- EI CI ČI CH, CH, (1) (2) (3) CH, CH, CH,Br H- CH CH CH CH CH, CH, (5) CH, (6) (4)…

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Q: Draw the Newman projection of the most stable conformation of pentane looking down the C2-C3 bond.

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Q: what  is  stereochemistry ?

A: Stereo-chemistry helps in determining the properties and reactions of the organic compounds. Drugs…

Q: what is the correct wedge dash line structure for D-galactose, include Hs wherever applicable,…

A: We have to draw the wedge-dash form of D-galactose.

Q: Choose whether the following structure is conjugated, nonconjugated, or cumulated. cumulated…

A: Conjugated system can be defined as the compound containing two double bonds which are separated by…

Q: whats the difference between regiochemistry, regioselective, and regiospecific, same thing with…

A: A question based on introduction to organic chemistry. Terms in organic chemistry about…

Q: Which of the two products has the chair conformation of greater stability? Explain.

A: As we know that chair conformations are the most precise representation of cyclohexane rings. In the…

Q: CO2H CO2H

A: In this question, we will see this compound is meso, chiral or achiral.  You can see details…

Q: Br

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Q: Draw the Newman projection so that it corresponds to the molecule and conformation shown when viewed…

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Q: Explain "Gauche conformations are generally higher in energy than anti conformations because of…

A: The stability of any conformation  depends upon   their energies as higher is the energy ,lesser is…

Q: Please draw a Newman projection, sighting down the carbon-2 to carbon-3 bond, forthe most stable…

A: Given molecule is, 2,3-dibromobutane.

Q: Naming the compound when in trans and cis conformation please explain

A: In this question we have to tell the name of the compound.

Q: Is it Endo or Exo?

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Q: In the the answer box, type the number of substituents that will be in the equatorial position in…

A: In the chair conformation of cyclohexane, there are two types of hydrogen atoms, axial and…

Q: Draw the Newman projection so that it corresponds to the molecule and conformation shown when viewed…

A: During Newman Projection drawing, we see along the carbon-carbon bond. To visualize the three…

Q: Cycloheptatriene (shown below) is non-aromatic because it A) does not have 4n+ 2 pi electrons. B) is…

A: For compound to be aromatic it must be Cylic Planer Fully conjugate  Contains (4n+2) pi electrons.…

Q: CI H H, H. H3CCH3 HH H H, CH3 H3C, H H, H3C H, H3C H 'CH3 CI I I I I

A: Steric strain or van der Waals strain is defined as the increases in potential energy when two atoms…

Q: Draw the structure of b-D-galactose molecule using  1C4 chair conformation.

A: Draw the structure of b-D-galactose molecule using  1C4 chair conformation.

Alkanes and Cycloalkanes

Alkanes are saturated organic compounds which are made up of C and H atoms. Alkanes have the general formula of CnH2n+2. Alkane contains sp3 hybridized carbon atoms with four sigmas (σ) bonds & every hydrogen atom is connected with one of the carbon atoms. The size of the alkane could be determined by the number of carbon atoms located in it.