![EBK GENERAL, ORGANIC, AND BIOLOGICAL CH](https://www.bartleby.com/isbn_cover_images/8220100853180/8220100853180_largeCoverImage.jpg)
Concept explainers
(a)
Interpretation:
Common name for the given ester has to be assigned.
Concept Introduction:
For naming an ester, it can be structurally viewed in a way that contains an acyl group and an alkyl group.
Rules to obtain IUPAC name and common name for an ester:
- Alkyl part appears first in the IUPAC name and it is followed by the acyl part of ester as a separate word.
- Name of the alkyl part in the ester is just a name of R group. It can be alkyl, cycloalkyl, or aryl group.
- Acyl part present in the ester is named by considering the acid name and replacing the suffix “-ic acid” with “-ate”.
- To obtain the common name the alkyl part name is the same while the acyl part name is derived from the common name of the acid by replacing the suffix “-ic acid” with “-ate”.
(b)
Interpretation:
Common name for the given ester has to be assigned.
Concept Introduction:
For naming an ester, it can be structurally viewed in a way that contains an acyl group and an alkyl group.
Rules to obtain IUPAC name and common name for an ester:
- Alkyl part appears first in the IUPAC name and it is followed by the acyl part of ester as a separate word.
- Name of the alkyl part in the ester is just a name of R group. It can be alkyl, cycloalkyl, or aryl group.
- Acyl part present in the ester is named by considering the acid name and replacing the suffix “-ic acid” with “-ate”.
- To obtain the common name the alkyl part name is the same while the acyl part name is derived from the common name of the acid by replacing the suffix “-ic acid” with “-ate”.
(c)
Interpretation:
Common name for the given ester has to be assigned.
Concept Introduction:
For naming an ester, it can be structurally viewed in a way that contains an acyl group and an alkyl group.
Rules to obtain IUPAC name and common name for an ester:
- Alkyl part appears first in the IUPAC name and it is followed by the acyl part of ester as a separate word.
- Name of the alkyl part in the ester is just a name of R group. It can be alkyl, cycloalkyl, or aryl group.
- Acyl part present in the ester is named by considering the acid name and replacing the suffix “-ic acid” with “-ate”.
- To obtain the common name the alkyl part name is the same while the acyl part name is derived from the common name of the acid by replacing the suffix “-ic acid” with “-ate”.
(d)
Interpretation:
Common name for the given ester has to be assigned.
Concept Introduction:
For naming an ester, it can be structurally viewed in a way that contains an acyl group and an alkyl group.
Rules to obtain IUPAC name and common name for an ester:
- Alkyl part appears first in the IUPAC name and it is followed by the acyl part of ester as a separate word.
- Name of the alkyl part in the ester is just a name of R group. It can be alkyl, cycloalkyl, or aryl group.
- Acyl part present in the ester is named by considering the acid name and replacing the suffix “-ic acid” with “-ate”.
- To obtain the common name the alkyl part name is the same while the acyl part name is derived from the common name of the acid by replacing the suffix “-ic acid” with “-ate”.
![Check Mark](/static/check-mark.png)
Want to see the full answer?
Check out a sample textbook solution![Blurred answer](/static/blurred-answer.jpg)
Chapter 16 Solutions
EBK GENERAL, ORGANIC, AND BIOLOGICAL CH
- Following are Fischer projection for a group of five carbon sugars,all of which are aldopentoses. Identify the pairs that are enantiomers and the pairs that are epimers.(The sugar shown herebare not all of the possible five carbon sugars.)arrow_forwardWhich form of lysine in Problem 18.56 is the zwitterion? What is the pI for the zwitterion?arrow_forwardWhich of the following is an anomer of a-D-galactopyranose? CH,OH он он он H он ÇH,OH OH он H он H он ÇH,OH он H. H OH он ÇH,OH OH он он он HHIarrow_forward
- Following are Fischer projections for a groupof five-carbon sugars, all of which are aldopentoses. Identify thepairs that are enantiomers and the pairs that are epimers. (Thesugars shown here are not all of the possible five-carbon sugars.)arrow_forwardFollowing are Fischer projections for a group of five-carbon sugars, all of which are aldopentoses. Identify the pairs that are enantiomers and the pairs that are epimers СНО СНО СНО H-C-OH H-C-OH H-C-OH H-C-OH Но-С—н H-C-OH H-C-OH Но-ҫ—н Но—с—н CHOH CHĻOH ČH,OH СНО СНО СНО Но —С— н H-C-OH HO-C-H Н—С—он Но -С—н HO-C-H H-c-OH H-C-OH HO-C-H CH̟OH ČHĻOH ČHĻOH Pairs of Enantiomers Pairs of Epimersarrow_forwardGentiobiose has the molecular formula C12H22O11 and has been isolated from gentian root and by hydrolysis of amygdalin. Gentiobiose exists in two different forms, one melting at 86°C and the other at 190°C. The lower melting form is dextrorotatory ([α] 16°), the higher melting one is levorotatory ([α] -6°). The rotation of an aqueous solution of either form, however, gradually changes until a final value of [α] 9.6° is observed. Hydrolysis of gentiobiose is efficiently catalyzed by emulsin and produces two moles of D-glucose per mole of gentiobiose. Gentiobiose forms an octamethylether, which on hydrolysis in dilute acid yields 2,3,4,6-tetra-O-methyl-D-glucose and 2,3,4-tri-O-methyl-D-glucose. What is the structure of gentiobiose? EXPLAIN IN DETAIL.arrow_forward
- D- and L- designations are used to distinguish between the two possible enantiomers of the monosaccharide, galactose. From the Fischer projection, determine the designation of this monosaccharide.arrow_forwardWhich of the following is a property of both D-altrose and D-talose?arrow_forwardDraw the structural formula for α-D-glucosyl-(1→6)-D-mannosamine,and circle the part of this structure that makes the compound a reducing sugar.arrow_forward
- Following are structural formulas for cytosine and thymine. Draw two additional tautomeric forms for cytosine and three additional tautomeric forms for thymine.arrow_forwardComplete the following table by providing the Fischer and Haworth Projections of the given sugars. In the Fischer Projection put an asterisk (*) mark in the chiral centers of the molecule. Sugar Fischer Projection Haworth Projection (Complete) alpha-anomer Haworth Projection (Abbreviated) beta-anomer D-Mannose D-Xylose L-Lyxosearrow_forwardDraw the Haworth projection of β-D-Altopyranose given the structure of D-Altrose.arrow_forward
- Principles Of Radiographic Imaging: An Art And A ...Health & NutritionISBN:9781337711067Author:Richard R. Carlton, Arlene M. Adler, Vesna BalacPublisher:Cengage Learning
![Text book image](https://www.bartleby.com/isbn_cover_images/9781337711067/9781337711067_smallCoverImage.jpg)