etermine the systematic (IUPAC) name for each of the molecules represented by the Newman projections below. Newman Projection H H H H3C CI CH3 I I Cl CH3 CH3 H H CH3 CH3 Br H H Explanation Check IUPAC Name ☐ © 2024 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center Acc
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- Write de complete (not UIPAC) name of each molecule below. Note: If a molecule is one of a pair of enantiomers, be sure you start its name with D- or L- so we know which enantiomer it is. molecule H₂N H₂N. HS NH3 NH3 common name (not the IUPAC name) 0 0Consider the molecule 1-bromo-2-methylbutane. C3 and C4 should be drawn as Et as in theexample. This group is called an ethyl group and can be considered a sphere about twice the sizeof a methyl group. Draw the following Newman projections sighting down the C1C2 bond... a. The lowest potential energy conformation. b. The highest potential energy staggered conformation.Be sure to answer all parts. Name the following compound according to substitutive IUPAC nomenclature. OH (select) (select) (select) (select) 7 of 11 Next> < Prev C F5 PrtSc F6 F4 F7 F10 F8 F9 F3 F11 F12 & # 4 3 7 9 0 CO LO AST
- Give the systematic (IUPAC) name for each molecule. CH3CCH3 systematic (IUPAC) name: CH3CH2CH2CCH3 systematic (IUPAC) name: terms of Use contact us help ebout us careers privacy policy 7:29 PMSUNY Old Westbury | Own X. O Student Home Bb Pearson's MyLab & Master X E MasteringChemistry: chap X A session.masteringchemistry.com/myct/itemView?assignmentProblemID=1855197092. Our knowledge of chair conformations allows us to use them to determine a great deal about a reaction's mechanism. In particular, using a t-butyl group to 'fix' a cyclohexane in a single conformation can help us learn about the spatial requirements and energetics of a reaction. Consider the following two reaction products: a. NO NID ALOH 1) NaCN 2) H+ 1) NaBH4 2) H3O+ OH Group -H -CN -OH A Value (kcal/mol) Defined as 0 0.2 kcal/mol 1.0 kcal/mol Draw the most stable chair conformation for each of the two products. b. Based on the A values in the table above, do the two products have the most stable conformation at the new stereocenter?[References) Draw the line-angle formula for the most stable carbocation with a molecular formula of: C3H,+ • You do not have to consider stereochemistry. You do not have to explicitly draw H atoms. • If there are alternative structures, draw the most stable one. P opy aste ChemDoodleWhich of these products is the result of a hydride shift occuring during the substitution reaction of aqueous 2-chloro-3-methylpentane? CH3CH2CCH2CH3 || CH2 CH3CH(OH)CH(CH3)CH2CH3 CH2=CHC(CH3)=CHCH3 CH3CH=C(CH3)CH2CH3 CH3CH2C(CH3)CH2CH3 | OH2. Our knowledge of chair conformations allows us to use them to determine a great deal about a reaction's mechanism. In particular, using a t-butyl group to 'fix' a cyclohexane in a single conformation can help us learn about the spatial requirements and energetics of a reaction. Consider the following two reaction products: CN 1) NaCN 2) H+ OH 1) NaBH4 2) H3O+ OH Group -H -CN A Value (kcal/mol) Defined as 0 0.2 kcal/mol -OH 1.0 kcal/mol c. For any products that do have the most stable conformation, does our understanding of the mechanism allow for ‘thermodynamic control'? d. If one of the products is not the most stable, can you explain the observed product based on ‘kinetic control'? (Does the most easily formed transition state result in the observed product?) Consider the chair-like conformation of the starting material.Prnhlem 2 Give IUPAC names for the following compounds: la) CI. „Br (b) CH3 NH2 CH2CH2CHCH3 Br Id) CI. CH3 (e) CH2CH3 CH3 CI O2N NO2 H3C CH3TConsider a Newman projection of 2-methylbutane shown. Calculate the energy from the strain present in this conformation. CH3 H3C. H Interaction Type gauche CH3-H gauche CH3-CH3 eclipsed CH3-H eclipsed CH3-CH3 H H CH3 Strain Energy (kcal/mol) 0.0 0.7 3.3 5.6 1 4 2 +/- LO 5 7 8 kcal/mol 3 CO 6 9 O X C x 100SEE MORE QUESTIONS