11. Starting with 1-bromopentane, make as many of the functional groups (nothing aromatic) as you can
11. Starting with 1-bromopentane, make as many of the functional groups (nothing aromatic) as you can
1. How many different carbon atoms are present in
1-bromopentane?
2. What types of carbons are present in 1-bromopentane?
3. How many different hydrogen atoms are present in
1-bromopentane?
4. What functional groups is the molecule hydrogens attached
or are part of? aka. carboxyilic acid as an example
5. How many CH hydrogens are present on each carbon based on
the integration and multiplicity?
6. How many CH2 Hydrogens are present on each carbon?
CH3?
200 180 160 140 120...
Please help me interpret the IR for
2-(3,4-dimethoxybenzylidene)-1-indnone. Which peaks represent
functional groups:
- Aromatic
- ketone
- Ester
- Alkene
1445 1295 12033 Os 106 127530109603 1528142097 1615 11 1464 34 1598 22 102062 1508 47 114099 54 51.37 4000.0 3000 2000 1500 cm-1
is ketone a functional group of this molecule?
Could you identify 3 functional groups
here, if they exist
Ам де Ketone LL AMide N..((s) EO - Aromatic
Which of the functional groups can act as a hydrogen bond donor? Select all that apply Amide Aromatic ring Carboxylic acid Amine Alcohol Ester Ether Ketone
"We now continue the introduction of organic chemistry roadmaps. Because of the many new functional groups that will be introduced in coming chapters, we recommend that you make a new roadmap to accommodate the reactions in Chapters 15–18.To make your own roadmap for Chapters 15–18, take a blank sheet of paper and write the following functional groups in the orientations shown. Fill the entire sheet of paper and leave plenty of room between functional groups. Most students find it helpful...
1) The structure for Prozac, a commonly prescribed antidepressant, is shown below. Identify the circled functional groups from left to right. a) amine, aromatic, ether b) amide, aromatic, ester c) nitrile, aromatic, alcohol d) amine, aromatic, alcohol F H-CI 2) Which reagent(s) would react with 1-bromopentane to form heptane (as shown below) in good yield? 1)? Br 2) H-О b) I, II, and II a) II and III CaLi MgBr Li d) III only c) I and II III I
Organic Synthesis. Starting materials can still have functional
groups. Can be solved in 4 steps or less, but not necessary. With
no starting material having MORE than C carbons. So, ignore what is
written on page/board in the parentheses (that was a
miss-wording)
Synthesize (with smallest starting material i) c=3 having c max carbons) jjii) <=3 c=7 iii) Ph my Y OH HO
One molecule of NaBH4 can in theory reduce four ketone functional groups. If you had 25 mg of NaBH4, how many many mg of benzil could be fully reduced?
How many functional groups do you need to consider to find the PI of the dipeptide lys-his?
What functional groups can you identify with Dioxin? aromatics alcohol ethers halogen esters carboxylic alkene What functional groups can you identify with Furan? halogen carboxylic esters ethers alcohol alkene aromatics What functional groups can you identify with Hexachlorobenzene? halogen aromatics esters ethers alkene alcohol carboxylic What functional groups can you identify with DDT? Check all that apply. alcohol halogen ethers alkene esters aromatics carboxylic