Concept explainers
(a)
Interpretation:
The IUPAC name for the given structure of acid chloride is to be provided.
Concept introduction:
The IUPAC name of a compound is written from its structure. The IUPAC name is made up of three parts: prefix, root, and suffix. The suffix indicates the highest-priority functional group present. Its location is written as a prefix, unless redundant. The root is the longest continuous carbon chain that also includes the highest priority functional group. The carbon atom of the highest functional group must be the part of the longest continuous chain of carbon atoms, and the numbering starts from that carbon. Any other
For acid chlorides, the highest priority functional group is the
If any chiral carbons are present, their absolute configurations are specified at the start along with the carbon number if necessary. A di, tri, etc., before a prefix or suffix indicates the number of instances of that functional group.
(b)
Interpretation:
The IUPAC name for the given structure of acid chloride is to be provided.
Concept introduction:
The IUPAC name of a compound is written from its structure. The IUPAC name is made up of three parts: prefix, root, and suffix. The suffix indicates the highest-priority functional group present. Its location is written as a prefix, unless redundant. The root is the longest continuous carbon chain that also includes the highest priority functional group. The carbon atom of the highest functional group must be the part of the longest continuous chain of carbon atoms, and the numbering starts from that carbon. Any other functional groups present are listed alphabetically as prefixes along with their locant numbers.
For acid chlorides, the highest priority functional group is the carboxylic acid chloride group (
(c)
Interpretation:
The IUPAC name for the given structure of acid chloride is to be provided.
Concept introduction:
The IUPAC name of a compound is written from its structure. The IUPAC name is made up of three parts: prefix, root, and suffix. The suffix indicates the highest-priority functional group present. Its location is written as a prefix, unless redundant. The root is the longest continuous carbon chain that also includes the highest priority functional group. The carbon atom of the highest functional group must be the part of the longest continuous chain of carbon atoms, and the numbering starts from that carbon. Any other functional groups present are listed alphabetically as prefixes along with their locant numbers.
For acid chlorides, the highest priority functional group is the carboxylic acid chloride group (

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Chapter F Solutions
EBK ORGANIC CHEMISTRY: PRINCIPLES AND M
- Curved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps. :0: NaOH, H₂O 00:4 Na O heat NaO Select to Add Arrows Select to Add Arrows :0: Na a NaOH, H2O :0: NaOH, H2O heat heat Na ONH Select to Add Arrowsarrow_forwardCurved arrows are used to illustrate the flow of electrons. Using the provided starting and product structures, draw the curved electron-pushing arrows for the following reaction or mechanistic step(s). Be sure to account for all bond-breaking and bond-making steps. H CH3NH3+ :0: :0: HO CH3NH2 HH iSelect to Add Arrows i Select to Add Arrows i HH CH3NH3+ CH3NH2 Select to Add Arrows i CH3NH3 CH3NH2 ايكدا HH Select to Add Arrowsarrow_forwardThe reaction is carried out with gases: A → B + C at 300 K. The total pressure is measured as a function of time (table). If the reaction order is 2, calculate the rate or kinetic constant k (in mol-1 L s¹) Ptotal (atm) 492 676 760 808 861 t(s) 0 600 1200 1800 3000arrow_forward
- can someone give a description of this NMR including whether its a triplt singlet doublet where the peak is around at ppm and what functional group it representsarrow_forward1. Determine the relationship between the following molecules as identical, diastereomers, or enantiomers (6 points, 2 points each). OH OH OH A-A OH HOT HO- ACHN and HO- ACHN OH HO HO ° OH and OH OH SH and ...SHarrow_forward20,0 Complete the electron pushing mechanism to y drawing the necomery unicaciones and carved on for Step 1: Add curved arms for the tint step, traiment with NalilĻ. The Nation 458 Step 2: Added for the second step, inalment with), how the "counterion bar Step 3: Daw the products of the last simplom organic and one incoganic spacient, including all nonbondingarrow_forward
- please provide the structure for this problem, thank you!arrow_forwardDraw the Fischer projection from the skeletal structure shown below. HO OH OH OH OH H Q Drawing Atoms, Bonds and Rings Charges I ☐ T HO H H OH HO I CH2OH H OH Drag H OH -CH2OH CHO -COOH Undo Reset Remove Donearrow_forwardplease provide the structure for this problem, thank youarrow_forward
- presented by Morallen Lig Intermine the hand product for the given mution by adding atoms, bonds, nonhonding diarion panda скуль Step 3: Comp the draw the product Step 2: Agama workup Compithe 429 ملولةarrow_forwardReaction A 0,0arrow_forwardpresented by Morillon Leaning Predict the organic product for the min кусур HSC Adithane carved arnown to come than that to the condon slchroruis in acid in in aquishri with ноюarrow_forward
