Question
the following structure is the substance Ritalin, a central nervous system stimulant. for each labeled carbon, draw out the hydrogens attached, if any and identify the carbon as either primary, secondary, or tertiary.

The following structure is the substance Ritalin, a central nervous system stimulant. For labeled carbon, draw out the hydrog
0 0
Add a comment Improve this question Transcribed image text
Answer #1

5:27 PM clH CH C-Cl one canon: 4/4 OCR Mark Rotate Recognize Note

Add a comment
Know the answer?
Add Answer to:
the following structure is the substance Ritalin, a central nervous system stimulant. for each labeled carbon, draw out...
Your Answer:

Post as a guest

Your Name:

What's your source?

Earn Coins

Coins can be redeemed for fabulous gifts.

Not the answer you're looking for? Ask your own homework help question. Our experts will answer your question WITHIN MINUTES for Free.
Similar Homework Help Questions
  • State the number of hydrogens bonded to each labeled carbon in the following substance and give...

    State the number of hydrogens bonded to each labeled carbon in the following substance and give its molecular formula. (The molecular formula answer is case-sensitive. The order of atoms should be carbon, then hydrogen, then others in alphabetical order.) a. Hydrogens at carbon a b. Hydrogens at carbon b c. Hydrogens at carbon The molecular formula is Submit Answer Try Another Version 10 item attempts remaining

  • need help with this questions U Label EACH carbon atom in the following structures as either primary (1°), secondary...

    need help with this questions U Label EACH carbon atom in the following structures as either primary (1°), secondary (2) tertiary f or quaternary (4) to trongly come from quaternary 4 I secondary 29 CH₃-CH₂-C CH₂ CH₂-CH₂-CH₂-CH₃ 2. NAME each of the following alcohols and then IDENTIFY each as either primary (1), secondary (29), or tertiary (3). 1º,2º Name or 3° CH3-CH-OH Cris Methana -3 1827 You prethol -3 162

  • ChemActivity 10: Oxidation and Reduction 145 Model 7: Primary (1°), Secondary (2°), and Tertiary (3°) Carbons...

    ChemActivity 10: Oxidation and Reduction 145 Model 7: Primary (1°), Secondary (2°), and Tertiary (3°) Carbons The words methyl (0'), primary (1), secondary (2"), and tertiary (3) were used to describe the number of (nonhydrogen) R groups attached to a carbocation carbon (see CA 8). This same naming strategy is used to describe any carbon with one attached "heteroatom," Z (hetero other). H R Z any atom other than C or H (hetroatom) R- -z -Z н- alkyl (not H)...

  • ChemActivity 10: Oxidation and Reduction 145 Model 7: Primary (1°), Secondary (2°), and Tertiary (3°) Carbons...

    ChemActivity 10: Oxidation and Reduction 145 Model 7: Primary (1°), Secondary (2°), and Tertiary (3°) Carbons The words methyl (0'), primary (1), secondary (2"), and tertiary (3) were used to describe the number of (nonhydrogen) R groups attached to a carbocation carbon (see CA 8). This same naming strategy is used to describe any carbon with one attached "heteroatom," Z (hetero other). H R Z any atom other than C or H (hetroatom) R- -z -Z н- alkyl (not H)...

  • 6. (a) Show the arrangement of the groups on the a carbon of the naturally occurring amino acids (draw out the stereoce...

    6. (a) Show the arrangement of the groups on the a carbon of the naturally occurring amino acids (draw out the stereocentre). (b) What is the significance of chirality in the biological world? 7. (a) Sh (a) Show the repeating unit of the polypeptide chain in a protein and indicate the peptide bond. (b) What are the following structures of a protein (i) primary, (ii) secondary, (iii) tertiary and (iv) quaternary. 1. Polypeptides are the natural polymer of the naturally...

  • 2. Draw structure (or) name the molecules according to IUPAC rules. (10 pt) i. 2,6-dimethyl-5-propyloctane Name...

    2. Draw structure (or) name the molecules according to IUPAC rules. (10 pt) i. 2,6-dimethyl-5-propyloctane Name the following compounds according to IUPAC nomenclature. ii. E: CH.CH C(CH3) 3. Give five different structures of CH3 alkyl groups, and identify the carbon at the point of attachment as primary, secondary or tertiary as appropriate. (10 pt)

  • Organization of the human nervous system is which of the following: a) Central nervoussystem / Peripheral...

    Organization of the human nervous system is which of the following: a) Central nervoussystem / Peripheral nervous system b) Peripheral nervous system / Somatic Nervoussystem c) Parasympathetic nervous system / Sympathetic nervous system d) Entericnervous system / Autonomic nervous system 7. Which of the following is not a structure of the Peripheral nervous system: a) gangliab) spinal cord c) sensory receptors d) cranial nerves 8.The Somatic nervous system relays sensory information from and motor response towhich type of tissue a)...

  • 16.) Within each of the following sets of alkyl radicals, name each radical; identify each as...

    16.) Within each of the following sets of alkyl radicals, name each radical; identify each as either primary, secondary, or tertiary; rank in order of decreasing stability; and sketch an orbital picture of the most stable radical, showing the hyper conjugative interaction(s). (a)   CH3CH2C·HCH3 and CH3CH2CH2CH2 · (b)   (CH3CH2)2CHCH2 · and (CH3CH2)2C·CH3 (c) (CH3)2CHC·HCH3 , (CH3)2C·CH2CH3 and (CH3)2CHCH2CH2· (I put the lone electron after the radical carbon.) Also, my main question is in bold. The rest I know and understand....

  • Draw one resonance structure for each of the conjugate bases formed by removal of the labeled...

    Draw one resonance structure for each of the conjugate bases formed by removal of the labeled protons (H4, H7, and H.) in acetanilide. Your structures should show all unshared electron pairs. Rank these protons in order of increasing acidity and explain the order you chose. нь N но Ha Acetanilide Part 1 out of 3 draw structure ... draw structure... draw structure ... H, removed H removed Hremoved Proline is an unusual amino acid because its Natom on the a...

  • Carbon-hydrogen bonds exhibit a range of different chemical reactivity that depends on molecular structure. Classify the...

    Carbon-hydrogen bonds exhibit a range of different chemical reactivity that depends on molecular structure. Classify the C-H bonds at the carbons labeled a-c in the structure below. Possible classifications are: primary, secondary, & tertiary or none if there are no hydrogens at the labeled carbon. C-H bond(s) at a C-H bond(s) at b or C-H bond(s) at v primary secondary tertiary 2 item attempts Submit Answer Try Another Version none 1-Bromopropane was prepared by heating 11.1 g of sodium bromide...

ADVERTISEMENT
Free Homework Help App
Download From Google Play
Scan Your Homework
to Get Instant Free Answers
Need Online Homework Help?
Ask a Question
Get Answers For Free
Most questions answered within 3 hours.
ADVERTISEMENT
ADVERTISEMENT
ADVERTISEMENT