The concept used to solve this problem is to locate the anomeric carbon in the given structure and then name the compound using the configuration.
If the given monosaccharide, –OH group and group are trans to each other, then it is called as anomer. Similarly, if –OH group and group are cis to each other, then it is called as anomer.
If the group is drawn up, then it is known as D-sugar. If the group is drawn down, then it is known as L-sugar.
Anomers are the two structural forms of same molecule which differentiate from each other only in the direction of the OH (hydroxyl) group present at the hemiacetal carbon.
Six-membered ring containing an oxygen atom is known as pyranose ring. Similarly, the five-membered ring containing an oxygen atom is known as furanose ring.
The structure is as follows:
This is a six-membered ring, so it is a pyranose.
The structure is as follows:
This is a six-membered ring, so it is a pyranose.
The structure is as follows:
This is a five-membered ring, so it is a furanose.
Ans:The name of the monosaccharide is .
The name of the monosaccharide is .
The name of the monosaccharide is .
Name the following Monosaccharides
me the following monosaccharides by placing the appropriate terms. CH2OH OH CH2OH H,OH OH OH CH2OH OH OH fructo galacto gluco pyranose ranaseD furanose
please help
Name the monosaccharides in the images by placing the appropriate terms. HOH -0 CH OH OH VOH Сн,он он HO CH2OH OH ОН OH O- @-galacto (pyrane O co pyramone - Pucto o | furanose Answer Bank a furanose Turanose p pyranse yranene
Give the systematic name for the following disaccharide by selecting the appropriate terms and filling in the blank number field.
Actes and weates) Actual fan2-11.00-2001/26 Complete the statements by placing the appropriate terms from the choices given In ye a butter is a solution containing a weak acid and its and its conjugale acid The munt of stronghase or acid that must be led to one liner of a buffer in order to change its pH by one it is an expressor
Name the following compounds. (Include
stereochemical terms where appropriate. Only use cis/trans
terminology for cyclic structures. Omit customary italics from your
name.)
Name the following compounds. (Include stereochemical terms where appropriate. Only use cis/trans terminology for cyclic structures. Omit customary italics from your name.) SH The IUPAC name is OH H3C H CH3 OH The IUPAC name is Submit Answer Try Another Version 8 item attempts remaining
4. Write the name of the following monosaccharides with the correct Stereoisomers (D or L). (3 marks) O с CH,OH H-C-OH CEO HOC-H HO-C-H T CHO HO-CH H-C-OH H-C-OH H-C-OH CH,OH H-C-OH CH,OH CH,OH В.
3. Draw by hand and name the following monosaccharides a. anomer of a-D-altrose b. enantiomer of D-altrose c. The pyranose and furanose forms of D-altrose d. The epimer of D-altrose e. A diasteroisomer of D-altrose f. What is the relationship between the following: - i. D-psicose and D-fructose - ii. D-fructose and D-sorbose - iii. glucose and sucrose - iv. a-D-glucopyranose and a-D-glucofuranoseType
2. Rank the following as indicated by placing the appropriate letter in the respective box a. Decreasing bond length of the indicated bond. shortest bond longest bond b. Increasing HOMO energy H3C-CH3 lowest HOMO highest HOMO
2. Rank the following as indicated by placing the appropriate letter in the respective box a. Decreasing bond length of the indicated bond. A longest bond shortest bond b. Increasing HOMO energy H3C-CH3 А в lowest HOMO highest HOMO
4. (5 pts.) Synthesize the following molecules by placing the appropriate reagents or intermediate in the boxes: a) 1 pt. 1 pt. OH 1 pt. 1/2 pt. each 1/2 pt. each NO2